MAGNESIUM ALUMINUM SILICATE
UNII 6M3P64V0NC

Substance Identification & Data

This profile provides standardized clinical and technical data for Magnesium Aluminum Silicate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 6M3P64V0NC.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 1327-43-1 and the RxNorm Concept ID (RxCUI) 17614. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
6M3P64V0NC
CAS Registry Number
1327-43-1
RxNorm Concept ID
17614

Detailed Substance Profile

Preferred Name
MAGNESIUM ALUMINUM SILICATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
6M3P64V0NC
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
C83898
National Cancer Institute reference terminology for clinical and research data.
Substance Type
mixture
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Magnesium Aluminum Silicate. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.

FDA Official Name

MAGNESIUM ALUMINUM SILICATE

Common Names & Synonyms

ALUMINII MAGNESII SILICAS [WHO-IP LATIN]
ALUMINIUM MAGNESIUM SILICATE
ALUMINIUM MAGNESIUM SILICATE [EP MONOGRAPH]
ALUMINIUM MAGNESIUM SILICATE [WHO-IP]
ALUMINIUM MAGNESIUM SILICATE HYDRATE
ALUMINIUM MAGNESIUM SILICATE POLYHYDRATE
ALUMINUM MAGNESIUM SILICATE
MAGNESIUM ALUMINIUM SILICATE
MAGNESIUM ALUMINIUM SILICATE HYDRATE
MAGNESIUM ALUMINUM SILICATE [II]
MAGNESIUM ALUMINUM SILICATE [VANDF]
MAGNESIUM ALUMINUM SILICATE [WHO-DD]
MAGNESIUM ALUMINUM SILICATE HYDRATE
MAGNESIUM ALUMINUM SILICATE HYDRATE [II]
MAGNESIUM ALUMINUM SILICATE, UNSPECIFIED
MAGNESIUM ALUMINUM SILICATE, UNSPECIFIED FORM
VEEGUM

Technical Codes

M-907015
MJ-2000

NDC Products Containing MAGNESIUM ALUMINUM SILICATE

This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:

Manufacturer Quick Index

Note: Due to the high number of listings (500), only Active Listings are currently displayed. Display is limited to the first 200 products.
→ A-S Medication Solutions 3
→ ACELLA PHARMACEUTICALS 1
→ AMERISOURCE BERGEN 1
→ ATLANTIC BIOLOGICALS CORP. 2
→ Acella Pharmaceuticals, LLC 6
→ Actavis Pharma, Inc. 1
→ Alchemee, LLC 4
→ Almay, Inc. 1
→ American Sales Company 1
→ Amneal Pharmaceuticals of New York LLC 1
→ Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals) 2
→ BURT'S BEES, INC. 1
→ BioComp Pharma, Inc. 8
→ Bioelements, Inc 1
→ Blistex Inc 1
→ Burel Pharmaceuticals, LLC 2
→ Burkhart Dental Supply Inc 12
→ Burt's Bees 2
→ CLINIQUE LABORATORIES LLC 1
→ CMP Pharma, Inc. 2
→ Camber Pharmaceuticals, Inc. 2
→ Cardinal Health 107, LLC 3
→ Chattem, Inc. 3
→ Combe Incorporated 1
→ Cosette Pharmaceuticals, Inc. 1
→ Crosstex International Inc. 10
→ Dharma Research, Inc. 1
→ Dharma Research, inc. 9
→ ESTEE LAUDER INC 1
→ Edenbridge Pharmaceuticals LLC. 2
→ Flageoli Limited 4
→ GOODSENSE 1
→ Galderma Laboratories, L.P. 2
→ GlaxoSmithKline LLC 12
→ H E B 2
→ Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 3
→ Hikma Pharmaceuticals USA Inc. 1
→ J. Strickland & Co. 2
→ J. Strickland and Co. 2
→ Kate Somerville Skincare, LLC 1
→ L'Oreal USA Products Inc 2
→ L. Perrigo Company 1
→ LG H&H CO., LTD. 2
→ LG HOUSEHOLD & HEALTH CARE LTD. 3
→ Laser Pharmaceuticals, LLC 1
→ Lupin Pharmaceuticals,Inc. 1
→ MAKEUP ART COSMETICS 1
→ Major Pharmaceuticals 2
→ Malin and Goetz Inc 1
→ Meijer Distribution Inc 1
→ Meijer Distribution, Inc 1
→ Mission Pharmacal Company 8
→ NorthStar RxLLC 1
→ Novel Laboratories, Inc. 1
→ P & L Development, LLC 1
→ PAI Holdings, LLC dba PAI Pharma 3
→ PTC Therapeutics, Inc. 1
→ Padagis Israel Pharmaceuticals Ltd 2
→ Padagis US LLC 1
→ Par Health USA, LLC 1
→ Person and Covey 3
→ Pharmaceutical Associates, Inc. 2
→ Philosophy, Inc. 1
→ REESE PHARMACEUTICAL CO. 1
→ Revlon Consumer Products Corp 3
→ Rugby Laboratories 4
→ SOHM, Inc 3
→ Safeway 1
→ Sun Pharmaceutical Industries, Inc. 3
→ TARGET CORPORATION 2
→ TARGET Corporation 1
→ THE PROACTIV COMPANY LLC 1
→ Target Corporation 1
→ Taro Pharmaceuticals U.S.A., Inc. 2
→ Teva Pharmaceuticals USA, Inc. 1
→ The Procter & Gamble Manufacturing Company 4
→ Topco Associates LLC 1
→ Topco Associates, LLC 1
→ UNITED NATURAL FOODS, INC. DBA UNFI 1
→ United Natural Foods, Inc. dba UNFI 1
→ Uriel Pharmacy Inc. 1
→ WALGREEN COMPANY 1
→ Wal-Mart Stores Inc 1
→ Wal-Mart Stores, Inc. 1
→ Walgreen Company 2
→ Walgreens 2
→ Wilshire Pharmaceuticals Inc. 2
→ Xttrium Laboratories, Inc. 1
→ e5 Pharma, LLC 1

A-S Medication Solutions

NDC Product
Human Prescription Drug

Nystatin
NDC 50090-1740

Generic Name
Nystatin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nystatin
NDC 50090-5315

Generic Name
Nystatin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Ammonium Lactate
NDC 50090-6587

Generic Name
Ammonium Lactate
Dosage Form
Lotion
Route
Topical
Marketing
ANDA
Active Listing

ACELLA PHARMACEUTICALS

NDC Product
Human Prescription Drug

Sodium Sulfacetamide - Sulfur Wash
NDC 42192-121

Generic Name
Sodium Sulfacetamide, Sulfur
Dosage Form
Liquid
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing

AMERISOURCE BERGEN

NDC Product
Human Otc Drug

Pinworm Treatment
NDC 46122-825

Generic Name
Pyrantel Pamoate
Dosage Form
Suspension
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

ATLANTIC BIOLOGICALS CORP.

NDC Product
Human Prescription Drug

Nystatin
NDC 17856-1045

Generic Name
Nystatin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Phenytoin
NDC 17856-4070

Generic Name
Phenytoin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

Acella Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Sodium Sulfacetamide And Sulfur Wash
NDC 42192-104

Generic Name
Sodium Sulfacetamide And Sulfur
Dosage Form
Liquid
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Sodium Sulfacetamide And Sulfur
NDC 42192-133

Generic Name
Sodium Sulfacetamide And Sulfur
Dosage Form
Solution
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Sodium Sulfacetamide 10 Sulfur 5 Cleanser
NDC 42192-136

Generic Name
Sulfacetamide Sodium And Sulfur
Dosage Form
Rinse
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Sodium Sulfacetamide 9 Sulfur 4.5 Wash
NDC 42192-144

Generic Name
Sulfacetamide Sodium And Sulfur
Dosage Form
Rinse
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Sodium Sulfacetamide 10 Sulfur 2 Cleanser
NDC 42192-147

Generic Name
Sulfacetamide Sodium And Sulfur
Dosage Form
Solution
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Actavis Pharma, Inc.

NDC Product
Human Prescription Drug

Griseofulvin
NDC 0472-0013

Generic Name
Griseofulvin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

Alchemee, LLC

NDC Product
Human Otc Drug

Proactiv Renewing Cleanser
NDC 11410-005

Generic Name
Benzoyl Peroxide
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Proactiv Repairing Treatment
NDC 11410-040

Generic Name
Benzoyl Peroxide
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Proactiv Solution Kit
NDC 11410-215

Generic Name
Solutions Kit
Dosage Form
Kit
Route
N/A
Marketing
OTC MONOGRAPH DRUG
Active Listing

Almay, Inc.

American Sales Company

NDC Product
Human Otc Drug

Careone Tioconazole 1
NDC 41520-426

Generic Name
Tioconazole
Dosage Form
Ointment
Route
Vaginal
Marketing
ANDA
Active Listing

Amneal Pharmaceuticals of New York LLC

NDC Product
Human Prescription Drug

Colesevelam Hydrochloride
NDC 0115-1864

Generic Name
Colesevelam Hydrochloride
Dosage Form
For Suspension
Route
Oral
Marketing
ANDA
Active Listing

Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals)

NDC Product
Human Prescription Drug

E.e.s
NDC 24338-134

Generic Name
Erythromycin Ethylsuccinate
Dosage Form
Granule, For Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

E.e.s
NDC 24338-136

Generic Name
Erythromycin Ethylsuccinate
Dosage Form
Granule, For Suspension
Route
Oral
Marketing
NDA
Active Listing

BURT'S BEES, INC.

BioComp Pharma, Inc.

NDC Product
Human Prescription Drug

Sodium Sulfacetamide, Sulfur
NDC 44523-520

Generic Name
Sulfacetamide Sodium, Sulfur
Dosage Form
Cream
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Sodium Sulfacetamide, Sulfur
NDC 44523-542

Generic Name
Sulfacetamide Sodium
Dosage Form
Cream
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Sodium Sulfacetamide, Sulfur
NDC 44523-550

Generic Name
Sulfacetamide Sodium, Sulfur
Dosage Form
Emulsion
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Sulfacetamide Sodium, Sulfur
NDC 44523-560

Generic Name
Sulfacetamide Sodium, Sulfur
Dosage Form
Emulsion
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Sulfacetamide Sodium
NDC 44523-568

Generic Name
Sulfacetamide Sodium
Dosage Form
Liquid
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Sodium Sulfacetamide And Sulfur
NDC 44523-600

Generic Name
Sulfacetamide Sodium, Sulfur
Dosage Form
Lotion
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Sodium Sulfacetamide And Sulfur
NDC 44523-624

Generic Name
Sulfacetamide Sodium, Sulfur
Dosage Form
Suspension
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Sodium Sulfacetamide And Sulfur
NDC 44523-748

Generic Name
Sodium Sulfacetamide 9.8% And Sulfur 4.8%
Dosage Form
Emulsion
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Bioelements, Inc

NDC Product
Human Otc Drug

Stage Fight Acne Mask
NDC 49825-137

Generic Name
Sulfur, Resorcinol
Dosage Form
Paste
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Blistex Inc

NDC Product
Human Otc Drug

Ivarest
NDC 10157-9077

Generic Name
Zinc Oxide, Benzyl Alcohol, And Diphenhydramine Hydrochlorid...
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Burel Pharmaceuticals, LLC

NDC Product
Human Otc Drug

Benzoyl Peroxide
NDC 35573-453

Generic Name
Benzoyl Peroxide
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Benzoyl Peroxide
NDC 35573-454

Generic Name
Benzoyl Peroxide
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Burkhart Dental Supply Inc

NDC Product
Human Prescription Drug

Burkhart
NDC 43498-100

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Burkhart
NDC 43498-101

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Burkhart
NDC 43498-102

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Burkhart
NDC 43498-103

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Burkhart
NDC 43498-104

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Burkhart
NDC 43498-105

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Burkhart
NDC 43498-106

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Burkhart
NDC 43498-107

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Burkhart
NDC 43498-108

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Burkhart
NDC 43498-109

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Burkhart Neutral Ph
NDC 43498-150

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Burkhart Neutral Ph
NDC 43498-151

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Burt's Bees

NDC Product
Human Otc Drug

Bb Broad Spectrum Spf 15 Light
NDC 26052-030

Generic Name
Zinc Oxide Titanium Dioxide
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Bb Broad Spectrum Spf 15 Medium
NDC 26052-032

Generic Name
Zinc Oxide Titanium Dioxide
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

CLINIQUE LABORATORIES LLC

CMP Pharma, Inc.

NDC Product
Human Prescription Drug

Sodium Polystyrene Sulfonate
NDC 46287-006

Generic Name
Sodium Polystyrene Sulfonate
Dosage Form
Suspension
Route
Oral; Rectal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atorvaliq
NDC 46287-030

Generic Name
Atorvaliq
Dosage Form
Suspension
Route
Oral
Marketing
NDA
Active Listing

Camber Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Nitrofurantoin
NDC 31722-491

Generic Name
Nitrofurantoin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Clobazam
NDC 31722-641

Generic Name
Clobazam
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

Cardinal Health 107, LLC

NDC Product
Human Prescription Drug

Nystatin
NDC 55154-4314

Generic Name
Nystatin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nystatin
NDC 55154-5788

Generic Name
Nystatin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Sodium Polystyrene Sulfonate
NDC 55154-7353

Generic Name
Sodium Polystyrene Sulfonate
Dosage Form
Suspension
Route
Oral; Rectal
Marketing
ANDA
Active Listing

Chattem, Inc.

NDC Product
Human Otc Drug

Selsun Blue 2-in-1
NDC 41167-1651

Generic Name
Selenium Sulfide
Dosage Form
Shampoo
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Selsun Blue Moisturizing
NDC 41167-6032

Generic Name
Selenium Sulfide
Dosage Form
Shampoo
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Selsun Blue Medicated
NDC 41167-6061

Generic Name
Selenium Sulfide
Dosage Form
Shampoo
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Combe Incorporated

NDC Product
Human Otc Drug

Vagistat
NDC 11509-0426

Generic Name
Tioconazole
Dosage Form
Ointment
Route
Vaginal
Marketing
ANDA
Active Listing

Cosette Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Griseofulvin
NDC 0713-0850

Generic Name
Griseofulvin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

Crosstex International Inc.

NDC Product
Human Prescription Drug

Zap Apf
NDC 24794-100

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Zap Apf
NDC 24794-101

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Zap Apf
NDC 24794-102

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Zap Apf
NDC 24794-103

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Zap Apf
NDC 24794-104

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Zap Apf
NDC 24794-105

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Zap Apf
NDC 24794-106

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Zap Apf
NDC 24794-107

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Zap Neutral
NDC 24794-108

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Zap Apf
NDC 24794-109

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Dharma Research, Inc.

NDC Product
Human Prescription Drug

Ionite Apf
NDC 53045-205

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental; Oral; Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Dharma Research, inc.

NDC Product
Human Prescription Drug

Ionite Apf
NDC 53045-200

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental; Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Ionite Apf
NDC 53045-201

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental; Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Ionite Apf
NDC 53045-202

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental; Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Ionite Apf
NDC 53045-203

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental; Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Ionite Apf
NDC 53045-204

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental; Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Ionite Apf
NDC 53045-206

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental; Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Ionite Apf
NDC 53045-207

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental; Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Ionite Apf Neutral
NDC 53045-235

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental; Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Ionite Apf Neutral
NDC 53045-237

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental; Oral; Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing

ESTEE LAUDER INC

Edenbridge Pharmaceuticals LLC.

NDC Product
Human Prescription Drug

Methenamine Mandelate
NDC 42799-105

Generic Name
Methenamine Mandelate
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Methenamine Mandelate
NDC 42799-106

Generic Name
Methenamine Mandelate
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Flageoli Limited

GOODSENSE

Galderma Laboratories, L.P.

NDC Product
Human Prescription Drug

Tri-luma
NDC 0299-5950

Generic Name
Fluocinolone Acetonide, Hydroquinone, And Tretinoin
Dosage Form
Cream
Route
Topical
Marketing
NDA
Active Listing

GlaxoSmithKline LLC

NDC Product
Human Prescription Drug

Lamictal
NDC 0173-0526

Generic Name
Lamotrigine
Dosage Form
Tablet, For Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lamictal
NDC 0173-0527

Generic Name
Lamotrigine
Dosage Form
Tablet, For Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lamictal
NDC 0173-0594

Generic Name
Lamotrigine
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lamictal
NDC 0173-0699

Generic Name
Lamotrigine
Dosage Form
Tablet, For Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lamictal Odt
NDC 0173-0772

Generic Name
Lamotrigine
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lamictal Odt
NDC 0173-0774

Generic Name
Lamotrigine
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lamictal Odt
NDC 0173-0776

Generic Name
Lamotrigine
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lamictal Odt
NDC 0173-0777

Generic Name
Lamotrigine
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lamictal Odt
NDC 0173-0778

Generic Name
Lamotrigine
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lamictal Odt
NDC 0173-0779

Generic Name
Lamotrigine
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lamictal Odt
NDC 0173-0780

Generic Name
Lamotrigine
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lamictal
NDC 0173-0817

Generic Name
Lamotrigine
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing

H E B

NDC Product
Human Otc Drug

Infants Non-staining Gas Relief
NDC 37808-014

Generic Name
Simethicone
Dosage Form
Solution/ Drops
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Tioconazole 1
NDC 37808-426

Generic Name
Tioconazole
Dosage Form
Ointment
Route
Vaginal
Marketing
ANDA
Active Listing

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Felodipine
NDC 23155-048

Generic Name
Felodipine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Felodipine
NDC 23155-049

Generic Name
Felodipine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Felodipine
NDC 23155-050

Generic Name
Felodipine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Hikma Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Naproxen
NDC 0054-3630

Generic Name
Naproxen
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

J. Strickland & Co.

NDC Product
Human Otc Drug

Sulfur 8 Kids Anti-dandruff
NDC 12022-023

Generic Name
Pyrithione Zinc
Dosage Form
Shampoo, Suspension
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Sulfur 8 Aqua Blue
NDC 12022-024

Generic Name
Pyrithione Zinc
Dosage Form
Shampoo, Suspension
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

J. Strickland and Co.

Kate Somerville Skincare, LLC

NDC Product
Human Otc Drug

Eradikate Acne Treatment
NDC 43479-106

Generic Name
Sulfur
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

L'Oreal USA Products Inc

L. Perrigo Company

NDC Product
Human Otc Drug

Good Sense Tioconazole 1
NDC 0113-0426

Generic Name
Tioconazole
Dosage Form
Ointment
Route
Vaginal
Marketing
ANDA
Active Listing

LG H&H CO., LTD.

LG HOUSEHOLD & HEALTH CARE LTD.

NDC Product
Human Otc Drug

Avon Beyond Glow Sun Moisturizer
NDC 53208-422

Generic Name
Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Laser Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Selenium Sulfide
NDC 16477-422

Generic Name
Selenium Sulfide
Dosage Form
Shampoo
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Lupin Pharmaceuticals,Inc.

NDC Product
Human Prescription Drug

Nitrofurantoin
NDC 43386-450

Generic Name
Nitrofurantoin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

MAKEUP ART COSMETICS

Major Pharmaceuticals

NDC Product
Human Prescription Drug

Nystatin
NDC 0904-7276

Generic Name
Nystatin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Childrens Acetaminophen
NDC 0904-7278

Generic Name
Acetaminophen
Dosage Form
Suspension
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Malin and Goetz Inc

NDC Product
Human Otc Drug

Malin And Goetz Acne Treatment
NDC 53634-010

Generic Name
Sulfur
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Meijer Distribution Inc

NDC Product
Human Otc Drug

Tioconazole 1
NDC 41250-426

Generic Name
Tioconazole
Dosage Form
Ointment
Route
Vaginal
Marketing
ANDA
Active Listing

Meijer Distribution, Inc

Mission Pharmacal Company

NDC Product
Human Prescription Drug

Avar-e Green
NDC 0178-0460

Generic Name
Sulfacetamide Sodium, Sulfur
Dosage Form
Cream
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Avar-e Ls
NDC 0178-0465

Generic Name
Sulfacetamide Sodium, Sulfur
Dosage Form
Cream
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Avar-e
NDC 0178-0470

Generic Name
Sulfacetamide Sodium, Sulfur
Dosage Form
Cream
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Avar Ls
NDC 0178-0475

Generic Name
Sulfacetamide Sodium, Sulfur
Dosage Form
Emulsion
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Avar
NDC 0178-0480

Generic Name
Sulfacetamide Sodium, Sulfur
Dosage Form
Emulsion
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Ovace Plus
NDC 0178-0490

Generic Name
Sulfacetamide Sodium
Dosage Form
Liquid
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Ovaceplus Plus
NDC 0178-0495

Generic Name
Sulfacetamide Sodium
Dosage Form
Cream
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Ovace Plus
NDC 0178-0620

Generic Name
Sulfacetamide Sodium
Dosage Form
Lotion
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing

NorthStar RxLLC

NDC Product
Human Prescription Drug

Clobazam
NDC 16714-087

Generic Name
Clobazam
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

Novel Laboratories, Inc.

NDC Product
Human Prescription Drug

Nitrofurantoin
NDC 40032-450

Generic Name
Nitrofurantoin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

P & L Development, LLC

NDC Product
Human Otc Drug

Stomach Relief Ultra Strength
NDC 49580-0842

Generic Name
Bismuth Subsalicylate
Dosage Form
Liquid
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

PAI Holdings, LLC dba PAI Pharma

NDC Product
Human Prescription Drug

Nystatin
NDC 0121-0868

Generic Name
Nystatin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Phenytoin
NDC 0121-0892

Generic Name
Phenytoin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nystatin
NDC 0121-1045

Generic Name
Nystatin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

PTC Therapeutics, Inc.

NDC Product
Human Prescription Drug

Emflaza
NDC 52856-505

Generic Name
Deflazacort
Dosage Form
Suspension
Route
Oral
Marketing
NDA
Active Listing

Padagis Israel Pharmaceuticals Ltd

NDC Product
Human Prescription Drug

Ammonium Lactate
NDC 45802-419

Generic Name
Ammonium Lactate
Dosage Form
Lotion
Route
Topical
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Ammonium Lactate
NDC 45802-493

Generic Name
Ammonium Lactate
Dosage Form
Cream
Route
Topical
Marketing
ANDA
Active Listing

Padagis US LLC

NDC Product
Human Prescription Drug

Trospium Chloride Er
NDC 0574-0118

Generic Name
Trospium Chloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Par Health USA, LLC

NDC Product
Human Prescription Drug

Diazoxide
NDC 0254-1010

Generic Name
Diazoxide
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

Person and Covey

NDC Product
Human Otc Drug

Dhs Zinc
NDC 0096-0735

Generic Name
Pyrithione Zinc
Dosage Form
Shampoo
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Dhs Zinc
NDC 0096-0811

Generic Name
Pyrithione Zinc
Dosage Form
Shampoo
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Dhs Body Wash
NDC 0096-0814

Generic Name
Zinc Pyrithione Wash
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Pharmaceutical Associates, Inc.

NDC Product
Human Prescription Drug

Nystatin
NDC 0121-0810

Generic Name
Nystatin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nystatin
NDC 0121-4810

Generic Name
Nystatin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

Philosophy, Inc.

REESE PHARMACEUTICAL CO.

NDC Product
Human Otc Drug

Pinworm Medicine
NDC 10956-778

Generic Name
Pyrantel Pamoate
Dosage Form
Suspension
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Revlon Consumer Products Corp

NDC Product
Human Otc Drug

Mitchum Roll On
NDC 10967-601

Generic Name
Aluminum Zirconium Tetrachlorohydrex Gly
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Hi And Dri Roll On
NDC 10967-786

Generic Name
Aluminum Chlorohydrate
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Hi And Dri Antiperspirant Roll On
NDC 10967-787

Generic Name
Aluminum Chlorohydrate
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Rugby Laboratories

NDC Product
Human Otc Drug

Rugby Anti-dandruff
NDC 0536-1995

Generic Name
Selenium Sulfide
Dosage Form
Shampoo
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

SOHM, Inc

Safeway

NDC Product
Human Otc Drug

Signature Care Tioconazole 1
NDC 21130-060

Generic Name
Tioconazole
Dosage Form
Ointment
Route
Vaginal
Marketing
ANDA
Active Listing

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Ammonium Lactate
NDC 51672-1300

Generic Name
Ammonium Lactate
Dosage Form
Lotion
Route
Topical
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Ammonium Lactate
NDC 51672-1301

Generic Name
Ammonium Lactate
Dosage Form
Cream
Route
Topical
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Phenytoin
NDC 51672-4069

Generic Name
Phenytoin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

TARGET CORPORATION

TARGET Corporation

NDC Product
Human Otc Drug

Digestive Relief Regular Strength
NDC 11673-372

Generic Name
Bismuth Subsalicylate
Dosage Form
Liquid
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

THE PROACTIV COMPANY LLC

NDC Product
Human Otc Drug

Proactiv Skin Purifying Mask
NDC 11410-013

Generic Name
Sulfur
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Target Corporation

NDC Product
Human Otc Drug

Up And Up Tioconazole 1
NDC 11673-426

Generic Name
Tioconazole
Dosage Form
Ointment
Route
Vaginal
Marketing
ANDA
Active Listing

Taro Pharmaceuticals U.S.A., Inc.

NDC Product
Human Prescription Drug

Nystatin
NDC 51672-4117

Generic Name
Nystatin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Clobazam
NDC 51672-4227

Generic Name
Clobazam
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Proglycem
NDC 0575-6200

Generic Name
Diazoxide
Dosage Form
Suspension
Route
Oral
Marketing
NDA
Active Listing

The Procter & Gamble Manufacturing Company

NDC Product
Human Otc Drug

Pepto-bismol
NDC 37000-438

Generic Name
Bismuth Subsalicylate
Dosage Form
Suspension
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Pepto-bismol Cherry
NDC 37000-439

Generic Name
Bismuth Subsalicylate
Dosage Form
Suspension
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Pepto-bismol Ultra
NDC 37000-440

Generic Name
Bismuth Subsalicylate
Dosage Form
Suspension
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Pepto-bismol Ultra Cherry
NDC 37000-441

Generic Name
Bismuth Subsalicylate
Dosage Form
Suspension
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Topco Associates LLC

NDC Product
Human Otc Drug

Topcare Tioconazole 1
NDC 36800-426

Generic Name
Tioconazole
Dosage Form
Ointment
Route
Vaginal
Marketing
ANDA
Active Listing

Topco Associates, LLC

NDC Product
Human Otc Drug

Infants Gas Relief
NDC 36800-119

Generic Name
Simethicone
Dosage Form
Solution/ Drops
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

UNITED NATURAL FOODS, INC. DBA UNFI

NDC Product
Human Otc Drug

Infants Gas Relief
NDC 41163-096

Generic Name
Simethicone
Dosage Form
Solution/ Drops
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

United Natural Foods, Inc. dba UNFI

NDC Product
Human Otc Drug

Equaline Tioconazole 1
NDC 41163-032

Generic Name
Tioconazole
Dosage Form
Ointment
Route
Vaginal
Marketing
ANDA
Active Listing

Uriel Pharmacy Inc.

NDC Product
Human Otc Drug

Borago Lavender
NDC 48951-2144

Generic Name
Borago Lavender
Dosage Form
Lotion
Route
Topical
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

WALGREEN COMPANY

NDC Product
Human Otc Drug

Walgreens 3 Step Acne System
NDC 0363-0153

Generic Name
Benzoyl Peroxide
Dosage Form
Kit
Route
N/A
Marketing
OTC MONOGRAPH DRUG
Active Listing

Wal-Mart Stores Inc

NDC Product
Human Otc Drug

Equate Tioconazole 1 Day
NDC 49035-426

Generic Name
Tioconazole
Dosage Form
Ointment
Route
Vaginal
Marketing
ANDA
Active Listing

Wal-Mart Stores, Inc.

Walgreen Company

NDC Product
Human Otc Drug

Tioconazole 1
NDC 0363-0426

Generic Name
Tioconazole
Dosage Form
Ointment
Route
Vaginal
Marketing
ANDA
Active Listing

Walgreens

NDC Product
Human Otc Drug

Soothe
NDC 0363-0073

Generic Name
Bismuth Subsalicylate
Dosage Form
Liquid
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Walgreens Pinworm Medicine
NDC 0363-0618

Generic Name
Pyrantel Pamoate
Dosage Form
Suspension
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Wilshire Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Erythromycin Ethylsuccinate
NDC 52536-134

Generic Name
Erythromycin Ethylsuccinate
Dosage Form
Granule, For Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Erythromycin Ethylsuccinate
NDC 52536-136

Generic Name
Erythromycin Ethylsuccinate
Dosage Form
Granule, For Suspension
Route
Oral
Marketing
NDA
Active Listing

Xttrium Laboratories, Inc.

NDC Product
Human Prescription Drug

Nystatin Oral Suspension
NDC 0116-4026

Generic Name
Nystatin
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

e5 Pharma, LLC

NDC Product
Human Prescription Drug

Diazoxide
NDC 13517-100

Generic Name
Diazoxide
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

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