.ALPHA.-TOCOPHEROL ACETATE, DL-
UNII WR1WPI7EW8

Substance Identification & Data

This profile provides standardized clinical and technical data for .alpha.-tocopherol Acetate, Dl-, uniquely identified by the FDA Unique Ingredient Identifier (UNII) WR1WPI7EW8.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 52225-20-4 and the RxNorm Concept ID (RxCUI) 317841. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
WR1WPI7EW8
CAS Registry Number
52225-20-4
RxNorm Concept ID
317841

Detailed Substance Profile

Preferred Name
.ALPHA.-TOCOPHEROL ACETATE, DL-
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
WR1WPI7EW8
The specific atomic composition represented as a molecular structure string.
InChIKey
C31H52O3
International Chemical Identifier digital signature for unique molecular identification.
SMILES String
ZAKOWWREFLAJOT-UHFFFAOYSA-N
Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
C74961
National Cancer Institute reference terminology for clinical and research data.
PubChem CID
2117
Unique identification number in the NCBI database of chemical substances.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
c12c(c(C)c(c(c1C)C)OC(=O)C)CCC(O2)(CCCC(CCCC(CCCC(C)C)C)C)C

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for .alpha.-tocopherol Acetate, Dl-. 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.

Common Names & Synonyms

.ALPHA.-TOCOPHEROL ACETATE, ALL-RACEMIC
.ALPHA.-TOCOPHEROL ACETATE, DL-
.ALPHA.-TOCOPHEROL ACETATE, DL- [II]
.ALPHA.-TOCOPHEROL ACETATE, DL-, DL-, DL-
.ALPHA.-TOCOPHERYL ACETATE, DL-
2H-1-BENZOPYRAN-6-OL, 3,4-DIHYDRO-2,5,7,8-TETRAMETHYL-2-((4R,8R)-4,8,12-TRIMETHYLTRIDECYL)-, 6-ACETATE, (2R)-REL-
ALL-RAC-ALFA-TOCOPHERYL ACETATE
ALL-RAC-ALPHA-TOCOPHERYL ACETATE
ALL-RAC-ALPHA-TOCOPHERYL ACETATE [FCC]
ALPHA-TOCOPHEROL ACETATE, DL-
ALPHA-TOCOPHERYL ACETATE, DL-
DL-.ALPHA.-TOCOPHEROL ACETATE
DL-.ALPHA.-TOCOPHEROL ACETATE [MI]
DL-.ALPHA.-TOCOPHERYL ACETATE
DL-ALPHA TOCOPHERYL ACETATE
DL-ALPHA TOCOPHERYL ACETATE [WHO-DD]
DL-ALPHA-TOCOPHERYL ACETATE
TOCOPHERYL ACETATE, DL-.ALPHA.
TOCOPHERYL ACETATE, DL-ALPHA
TOCOPHERYL ACETATE,DL-ALPHA [VANDF]

Technical Codes

J262.912G

NDC Products Containing .ALPHA.-TOCOPHEROL ACETATE, DL-

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 1
→ Acella Pharmaceuticals, LLC 2
→ Autumn Harp 5
→ Autumn Harp, Inc. 1
→ Beiersdorf Inc 2
→ Bio-Medical & Pharmaceutical Manufacturing Corporation 4
→ CLINIQUE LABORATORIES LLC 1
→ CVS Health 2
→ Coloplast Corp 2
→ Combe Incorporated 2
→ Cosco International, Inc 1
→ Cosco International, Inc. 1
→ Dharma Research, inc. 9
→ Dickinson Brands Inc. 1
→ Discount Drug Mart 2
→ Dolgencorp Inc 1
→ Empack Spraytech Inc. 1
→ Exeltis USA, Inc. 3
→ Focus Health Group 2
→ GIOVANNI COSMETICS INC 4
→ Ganzhou Olivee Cosmetic Co., Ltd. 2
→ Genuine Virgin Aloe Corporation 1
→ Guna spa 1
→ Humco Holding Group, Inc. 1
→ Kutol Products Company, Inc. 1
→ LG H&H CO., LTD. 1
→ LG H&H Co., Ltd. 3
→ LG H&H Co.,Ltd. 2
→ Method Pharmaceuticals, LLC 3
→ PURKLENZ FORMULATIONS INC. 1
→ Padagis Israel Pharmaceuticals Ltd 1
→ Patrin Pharma, Inc. 1
→ Port Jervis Laboratories, Inc. 1
→ PureTek Corporation 22
→ Randob Labs,Ltd. 1
→ Rite Aid 1
→ SHISEIDO AMERICAS CORPORATION 83
→ Sandoz Inc 2
→ Seton Pharmaceuticals 2
→ Shiseido Americas Corporation 1
→ TAI GUK PHARM. CO., LTD 1
→ Tai Guk Pharm. Co., Ltd. 6
→ Tai Guk Pharma. Co., Ltd. 1
→ Topco Associates LLC 1
→ Topiderm, Inc. 2
→ U.S. PHARMACEUTICAL CORPORATION 1
→ Unipack, Inc. 1
→ Wal-Mart Stores, Inc. 1
→ WalMart 1
→ Walgreen Co. 1
→ Walgreen Company 4
→ derma e 2

A-S Medication Solutions

NDC Product
Human Prescription Drug

Prenatal Vitamins Plus Low Iron
NDC 50090-0616

Generic Name
Prenatal With Ferrous Fumarate And Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Acella Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Pnv-select
NDC 42192-320

Generic Name
Vitamin A Acetate, Ascorbic Acid, Cholecalciferol, Alpha-toc...
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Pnv-dha
NDC 42192-321

Generic Name
Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol Acetate, ...
Dosage Form
Capsule, Gelatin Coated
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Autumn Harp

Autumn Harp, Inc.

NDC Product
Human Otc Drug

Barrier Balm
NDC 51514-0363

Generic Name
Barrier Balm
Dosage Form
Ointment
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Beiersdorf Inc

NDC Product
Human Otc Drug

Nivea Men Maximum Hydration Face
NDC 10356-567

Generic Name
Avobenzone, Octisalate, Octocrylene
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Nivea Men Sensitive Protective
NDC 10356-575

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

Bio-Medical & Pharmaceutical Manufacturing Corporation

NDC Product
Human Otc Drug

Pro-tect Sunscreen For Professionals
NDC 37945-860

Generic Name
Meradimate, Octinoxate, Octisalate, Oxybenzone
Dosage Form
Lotion
Route
Cutaneous
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Pro-tect Sports Sunscreen
NDC 37945-862

Generic Name
Meradimate, Octinoxate, Octisalate, Oxybenzone
Dosage Form
Lotion
Route
Cutaneous
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Pro-tect Sports Sunscreen
NDC 37945-862

Generic Name
Meradimate, Octinoxate, Octisalate, Oxybenzone
Dosage Form
Lotion
Route
Cutaneous
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Drug For Further Processing

NDC 37945-862

Generic Name
Meradimate, Octinoxate, Octisalate, Oxybenzone
Dosage Form
Lotion
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing

CLINIQUE LABORATORIES LLC

CVS Health

NDC Product
Human Otc Drug

Cvs Daily Dandruff Anti-dandruff
NDC 51316-178

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

Coloplast Corp

NDC Product
Human Otc Drug

Baza Protect
NDC 11701-082

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

Critic-aid Clear
NDC 11701-083

Generic Name
Petrolatum
Dosage Form
Ointment
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Combe Incorporated

Cosco International, Inc

NDC Product
Human Otc Drug

Oars And Alps Muscle Recovery Balm
NDC 52261-6300

Generic Name
Menthol, Methyl Salicylate
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Cosco International, Inc.

NDC Product
Human Otc Drug

Asystem Radical Relief Gel Roll-on
NDC 52261-4902

Generic Name
Menthol, Methyl Salicylate
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
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

Dickinson Brands Inc.

NDC Product
Human Otc Drug

Tn Dickinsons Pain And Itch Relief
NDC 52651-056

Generic Name
Pramoxine Hydrochloride And Zinc Acetate
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Discount Drug Mart

NDC Product
Human Otc Drug

Freds Medicated Anti Itch
NDC 53943-265

Generic Name
Pramoxine Hydrochloride, Menthol
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Dolgencorp Inc

Empack Spraytech Inc.

NDC Product
Human Otc Drug

Hand Sanitizer Zytec Germ Buster
NDC 50021-009

Generic Name
Alcohol 70%v/v
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Exeltis USA, Inc.

NDC Product
Human Prescription Drug

Select-ob Plus Dha Prenatal Supplement Plus Dha
NDC 0642-0075

Generic Name
.beta.-carotene, Vitamin A Acetate, Ascorbic Acid, Cholecalc...
Dosage Form
Kit
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Vitafol Ultra
NDC 0642-0093

Generic Name
Doconexent, Niacinamide, .alpha.-tocopherol Acetate, Dl-, Ch...
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Vitafol Fe Plus
NDC 0642-7473

Generic Name
Doconexent, Niacinamide, .alpha.-tocopherol Acetate, Dl-, Ch...
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Focus Health Group

NDC Product
Human Otc Drug

Anecream
NDC 24357-701

Generic Name
Lidocaine 4%
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anecream 5
NDC 24357-702

Generic Name
Lidocaine 5%
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

GIOVANNI COSMETICS INC

Ganzhou Olivee Cosmetic Co., Ltd.

Genuine Virgin Aloe Corporation

NDC Product
Human Otc Drug

Triderma Psoriasis Control
NDC 10738-980

Generic Name
Salicylic Acid
Dosage Form
Shampoo
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Guna spa

NDC Product
Human Otc Drug

Guna-cell
NDC 17089-450

Generic Name
Acetylcarnitine, L-ampc-alpha-lipoic Ac-a-tocopherol-ascorbi...
Dosage Form
Solution/ Drops
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Humco Holding Group, Inc.

NDC Product
Human Otc Drug

Humco Mineral Oil Heavy
NDC 0395-1685

Generic Name
Mineral Oil
Dosage Form
Liquid
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Kutol Products Company, Inc.

NDC Product
Human Otc Drug

Santi-gel Instant Hand Sanitizer
NDC 50865-056

Generic Name
Santi-gel Instant Hand Sanitizer
Dosage Form
Solution
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

LG H&H CO., LTD.

NDC Product
Human Otc Drug

Pop Feeling Peachy
NDC 53208-572

Generic Name
Sodium Fluoride
Dosage Form
Paste, Dentifrice
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing

LG H&H Co., Ltd.

NDC Product
Human Otc Drug

Pop Hint Of Mint
NDC 53208-571

Generic Name
Sodium Fluoride
Dosage Form
Paste, Dentifrice
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Pop Gel Pumpin Strawberry
NDC 53208-581

Generic Name
Sodium Fluoride
Dosage Form
Paste, Dentifrice
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Pop Gel Whatzzup Watermelon
NDC 53208-582

Generic Name
Sodium Fluoride
Dosage Form
Paste, Dentifrice
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing

LG H&H Co.,Ltd.

Method Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Multivitamin With Fluoride
NDC 58657-163

Generic Name
.alpha.-tocopherol Acetate, Dl-, Ascorbic Acid, Cyanocobalam...
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Multivitamin With Fluoride
NDC 58657-164

Generic Name
.alpha.-tocopherol Acetate, Dl-, Ascorbic Acid, Cyanocobalam...
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Multivitamin With Fluoride
NDC 58657-165

Generic Name
.alpha.-tocopherol Acetate, Dl-, Ascorbic Acid, Cyanocobalam...
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

PURKLENZ FORMULATIONS INC.

NDC Product
Human Otc Drug

Recovery Numb
NDC 49436-099

Generic Name
Lidocaine 4%
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Padagis Israel Pharmaceuticals Ltd

NDC Product
Human Prescription Drug

Mupirocin
NDC 45802-112

Generic Name
Mupirocin
Dosage Form
Ointment
Route
Topical
Marketing
ANDA
Active Listing

Patrin Pharma, Inc.

NDC Product
Human Prescription Drug

Prenatal Plus Vitamins
NDC 39328-106

Generic Name
Prenatal With Ferrous Fumarate And Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Port Jervis Laboratories, Inc.

PureTek Corporation

NDC Product
Human Prescription Drug

Multitol-m
NDC 59088-005

Generic Name
Multivitamin, Folate
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Finazol
NDC 59088-008

Generic Name
Ferrous Fumarate, Folate
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Prenatol-m
NDC 59088-009

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

Flotrex
NDC 59088-015

Generic Name
Multivitamins, Sodium Fluoride 0.5 Mg
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Flotrex
NDC 59088-017

Generic Name
Multivitamins, Sodium Fluoride 0.25 Mg
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Multivitamin
NDC 59088-018

Generic Name
Multivitamin
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Flotrex
NDC 59088-020

Generic Name
Multivitamins, Sodium Fluoride 1 Mg
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Menatrol
NDC 59088-156

Generic Name
Folate, Multivitamin
Dosage Form
Capsule
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Davimet-m
NDC 59088-158

Generic Name
Multivitamin
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Davimet With Iron
NDC 59088-160

Generic Name
Iron, Folate
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Diatrol
NDC 59088-162

Generic Name
Vitamins And Mineral
Dosage Form
Capsule
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Vitrexyl Plus Iron
NDC 59088-165

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Prenatrix
NDC 59088-166

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Vitrexate Fe
NDC 59088-168

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Prenatryl
NDC 59088-169

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Davimet With Fluoride
NDC 59088-170

Generic Name
Multivitamin, Fluoride
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Vitranol Fe
NDC 59088-173

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Venexa
NDC 59088-176

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

Venexa Fe
NDC 59088-177

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Pretrate
NDC 59088-178

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Zintrexyl-c
NDC 59088-180

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Folitin-z
NDC 59088-181

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Randob Labs,Ltd.

NDC Product
Human Otc Drug

Balmex Multi-purpose
NDC 52412-450

Generic Name
Petrolatum
Dosage Form
Ointment
Route
Topical
Marketing
OTC MONOGRAPH FINAL
Active Listing

Rite Aid

SHISEIDO AMERICAS CORPORATION

NDC Product
Human Otc Drug

Shiseido Benefiance Nutriperfect Day
NDC 58411-351

Generic Name
Avobenzone, Octinoxate, And Octocrylene
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Shiseido Benefiance Wrinkle Smoothing Day
NDC 58411-439

Generic Name
Avobenzone, Homosalate, Octinoxate, Octocrylene, And Oxybenz...
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Cle De Peau Beaute Protective Fortifying N
NDC 58411-454

Generic Name
Avobenzone, Octinoxate, Octocrylene, And Oxybenzone
Dosage Form
Emulsion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Shiseido The Makeup Foundation I20
NDC 58411-458

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

Shiseido The Makeup Foundation I40
NDC 58411-459

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

Shiseido The Makeup Foundation I60
NDC 58411-460

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

Shiseido The Makeup Foundation B20
NDC 58411-461

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

Shiseido The Makeup Foundation B40
NDC 58411-462

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

Shiseido White Lucent Day
NDC 58411-463

Generic Name
Avobenzone, Octinoxate, And Octocrylene
Dosage Form
Emulsion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Shiseido The Makeup Foundation B60
NDC 58411-534

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

Cle De Peau Beaute Protective Fortifying N
NDC 58411-562

Generic Name
Avobenzone, Octinoxate, Octocrylene, And Oxybenzone
Dosage Form
Emulsion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Shiseido Benefiance Wrinkleresist24 Day
NDC 58411-628

Generic Name
Avobenzone, Octinoxate, And Octocrylene
Dosage Form
Emulsion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Shiseido Benefiance Wrinkleresist24 Day
NDC 58411-629

Generic Name
Avobenzone, Octinoxate, And Octocrylene
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Cle De Peau Beaute Concealer N 1
NDC 58411-658

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

Cle De Peau Beaute Concealer N 2
NDC 58411-659

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

Cle De Peau Beaute Concealer N 3
NDC 58411-660

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

Cle De Peau Beaute Concealer N 4
NDC 58411-661

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

Cle De Peau Beaute Concealer N 5
NDC 58411-662

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

Cle De Peau Beaute Concealer N 7
NDC 58411-663

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

Cle De Peau Beaute Concealer N 8
NDC 58411-664

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

Cle De Peau Beaute Concealer N 9
NDC 58411-665

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

Cle De Peau Beaute Concealer N 10
NDC 58411-666

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

Cle De Peau Beaute Concealer N 11
NDC 58411-667

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

Cle De Peau Beaute Concealer N 12
NDC 58411-668

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

Cle De Peau Beaute Concealer N 13
NDC 58411-669

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

Shiseido Revitalessence Skin Glow Primer
NDC 58411-894

Generic Name
Avobenzone, Octinoxate, And Octocrylene
Dosage Form
Emulsion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Shiseido Future Lx Universal Defense S
NDC 58411-902

Generic Name
Octisalate, Octocrylene, And Zinc Oxide
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Sandoz Inc

NDC Product
Human Otc Drug

Cetirizine Hydrochloride
NDC 0781-5283

Generic Name
Cetirizine Hydrochloride
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Cetirizine Hydrochloride
NDC 0781-5284

Generic Name
Cetirizine Hydrochloride
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
ANDA
Active Listing

Seton Pharmaceuticals

NDC Product
Human Prescription Drug

Se-natal 19
NDC 13925-116

Generic Name
.beta.-carotene, Ascorbic Acid, Cholecalciferol, .alpha.-toc...
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Se-natal 19 Chewable
NDC 13925-117

Generic Name
Vitamins And Minerals
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Shiseido Americas Corporation

NDC Product
Human Otc Drug

Cle De Peau Beaute Uv Protective N
NDC 58411-905

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

TAI GUK PHARM. CO., LTD

NDC Product
Human Otc Drug

Pop Feeling Peachy
NDC 43136-512

Generic Name
Sodium Fluoride
Dosage Form
Paste, Dentifrice
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing

Tai Guk Pharm. Co., Ltd.

NDC Product
Human Otc Drug

Pop Hint Of Mint
NDC 43136-511

Generic Name
Sodium Fluoride
Dosage Form
Paste, Dentifrice
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Pop Gel Pumpin Strawberry
NDC 43136-521

Generic Name
Sodium Fluoride
Dosage Form
Paste, Dentifrice
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Pop Gel Whatzzup Watermelon
NDC 43136-522

Generic Name
Sodium Fluoride
Dosage Form
Paste, Dentifrice
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing

Tai Guk Pharma. Co., Ltd.

Topco Associates LLC

Topiderm, Inc.

NDC Product
Human Otc Drug

Dr. Zenovia Spot Treatment
NDC 51326-802

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

Dr. Zenovia Acne Cleanser
NDC 51326-803

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

U.S. PHARMACEUTICAL CORPORATION

NDC Product
Human Otc Drug

V-bella
NDC 52747-155

Generic Name
Boric Acid
Dosage Form
Suppository
Route
Vaginal
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Unipack, Inc.

NDC Product
Human Otc Drug

Natures Choice Vitamins A And D
NDC 43749-230

Generic Name
A And D Ointment
Dosage Form
Ointment
Route
Topical
Marketing
OTC MONOGRAPH FINAL
Active Listing

Wal-Mart Stores, Inc.

WalMart

NDC Product
Human Otc Drug

Jock Itch Clotrimazole Antifungal
NDC 49035-837

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

Walgreen Co.

Walgreen Company

NDC Product
Human Otc Drug

Walgreens Pain Relieving Foot Pain Relief
NDC 0363-9379

Generic Name
Apis Mellifera, Gelsemium Sempervirens Whole, And Pseudognap...
Dosage Form
Cream
Route
Topical
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

derma e

NDC Product
Human Otc Drug

Derma E Eczema Relief
NDC 54108-8712

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

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