DIMETHICONE 350
UNII 2Y53S6ATLU

Substance Identification & Data

This profile provides standardized clinical and technical data for Dimethicone 350, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 2Y53S6ATLU.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9006-65-9 and the RxNorm Concept ID (RxCUI) 1363569. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
2Y53S6ATLU
CAS Registry Number
9006-65-9
RxNorm Concept ID
1363569

Detailed Substance Profile

Preferred Name
DIMETHICONE 350
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
2Y53S6ATLU
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
C83674
National Cancer Institute reference terminology for clinical and research data.
Substance Type
polymer
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Dimethicone 350. 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

DIMETHICONE 350

Common Names & Synonyms

DIMETHICONE (350 CST)
DIMETHICONE (350 MPA.S)
DIMETHICONE 350 [II]
DIMETHICONE 350 [USAN]
DIMETICONE (350 CST)
DIMETICONE 350
DIMETICONE 350 [EP IMPURITY]

Brand / Trade Names

DOW CORNING 360 MEDICAL FLUID (350 CST)
DOW CORNING Q7-9120 SILICONE FLUID (350 CST)

NDC Products Containing DIMETHICONE 350

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 (205), only Active Listings are currently displayed.
→ A-S Medication Solutions 3
→ American Health Packaging 1
→ Amerisource Bergen 1
→ Better Living Brands LLC 1
→ Bryant Ranch Prepack 1
→ CARDINAL HEALTH 1
→ CDMA 2
→ CHAIN DRUG MARKETING ASSOCIATION, INC. 1
→ CLEURE 1
→ CVS 1
→ CVS Health 1
→ CVS Pharmacy 1
→ Camber Pharmaceuticals, Inc. 7
→ Cardinal Health 1
→ Chain Drug Marketing Association, Inc. 1
→ Chartwell RX, LLC. 1
→ Cosco International, Inc. 16
→ DISCOUNT DRUG MART, INC. 1
→ Derma Care Research Labs, LLC 3
→ Derma Care Research Labs,LLC 1
→ Dr. Reddy's Laboratories Inc 3
→ Dr. Reddy's Laboratories Inc. 2
→ Dr. Reddys Laboratories Inc 3
→ E-Z-EM Canada Inc 5
→ E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. 1
→ Front Line Safety 1
→ Genus Lifesciences Inc. 1
→ Glenmark Pharmaceuticals Inc., USA 1
→ H E B 1
→ Herbalife International of America, Inc. 1
→ Hikma Pharmaceuticals USA Inc. 1
→ HyVee Inc 1
→ Incyte Corporation 1
→ Just Brands LLC 1
→ KROGER COMPANY 1
→ Kobayashi Healthcare International, Inc. 1
→ Kramer Laboratories 2
→ Kroger Company 1
→ Medline Industries, LP 1
→ NorthStar RxLLC 7
→ ProStat First Aid LLC 3
→ Proper Buys LLC 1
→ PureTek Corporation 1
→ RENU LABORATORIES, LLC 3
→ Randob Labs, LTD 1
→ Rite Aid Corporation 1
→ SJOLIE, INC. 1
→ Sage Products LLC 1
→ SpecGx LLC 7
→ Steel City Health Private Limited 1
→ Sun Pharmaceutical Industries, Inc. 3
→ Sunstation USA, LLC 1
→ TRUTEK CORP. 2
→ Tender Corporation d/b/a Adventure Ready Brands 2
→ Teva Pharmaceuticals USA, Inc. 3
→ The J. Molner Company LLC 1
→ Veridian Healthcare 4
→ WALGREENS COMPANY 1
→ WESTLAKE HB PHARMA 1
→ WINCO FOODS, LLC 1
→ Walgreens 2
→ Weeks & Leo Compnay, INC. 1
→ Westlake Pharma LLC 1
→ iON Pharma, LLC 2

A-S Medication Solutions

NDC Product
Human Prescription Drug

Atomoxetine
NDC 50090-6127

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 50090-6143

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 50090-6144

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

American Health Packaging

NDC Product
Human Prescription Drug

Rufinamide
NDC 60687-824

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

Amerisource Bergen

NDC Product
Human Otc Drug

Good Neighbor Roll-on Pain Relief
NDC 46122-802

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

Better Living Brands LLC

NDC Product
Human Otc Drug

Signature Care Lidocaine Cream
NDC 21130-544

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

Bryant Ranch Prepack

NDC Product
Human Prescription Drug

Clobetasol Propionate (emollient)
NDC 72162-2628

Generic Name
Clobetasol Propionate
Dosage Form
Cream
Route
Topical
Marketing
ANDA
Active Listing

CARDINAL HEALTH

NDC Product
Human Otc Drug

Leader Lidocaine
NDC 70000-0099

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

CDMA

NDC Product
Human Otc Drug

Qc Spf 50 Sunscreen
NDC 63868-531

Generic Name
Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10...
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Qc Spf 30 Sunscreen
NDC 63868-913

Generic Name
Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 6%
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

CHAIN DRUG MARKETING ASSOCIATION, INC.

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 83324-200

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

CLEURE

NDC Product
Human Otc Drug

Spf 30 Sunscreen
NDC 83294-101

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

CVS

NDC Product
Human Otc Drug

Cvs Anti-itch
NDC 69842-263

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

CVS Health

NDC Product
Human Otc Drug

Cvs Health Lidocaine Cream
NDC 69842-814

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

CVS Pharmacy

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 51316-563

Generic Name
Esomeprazole Magnesium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Camber Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Atomoxetine
NDC 31722-714

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 31722-715

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 31722-716

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 31722-717

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 31722-718

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 31722-719

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 31722-720

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Cardinal Health

NDC Product
Human Otc Drug

Leader
NDC 70000-0098

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

Chain Drug Marketing Association, Inc.

NDC Product
Human Otc Drug

Quality Choice
NDC 83324-297

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

Chartwell RX, LLC.

NDC Product
Human Prescription Drug

Calcium Acetate
NDC 62135-191

Generic Name
Calcium Acetate
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Cosco International, Inc.

NDC Product
Human Otc Drug

Carpe Antiperspirant For Hands
NDC 52261-4701

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

Carpe Antiperspirant For Underarms
NDC 52261-4703

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

Carpe Antiperspirant Underarm
NDC 52261-4721

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

DISCOUNT DRUG MART, INC.

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 53943-039

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Derma Care Research Labs, LLC

NDC Product
Human Otc Drug

Aruba Sun Spf 50 Sunscreen
NDC 72839-083

Generic Name
Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10...
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Habana Brisa Spf 30 Sunscreen
NDC 72839-215

Generic Name
Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 6%
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Aruba Sun Spf 70 Sunscreen
NDC 72839-915

Generic Name
Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10...
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Derma Care Research Labs,LLC

NDC Product
Human Otc Drug

Aruba Sun Spf 30 Sunscreen
NDC 72839-137

Generic Name
Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 6%
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Dr. Reddy's Laboratories Inc

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 43598-067

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 43598-327

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 43598-926

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Dr. Reddy's Laboratories Inc.

NDC Product
Drug For Further Processing

NDC 43598-327

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing

NDC 43598-926

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing

Dr. Reddys Laboratories Inc

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 43598-069

Generic Name
Esomeprazole Magnesium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 75907-119

Generic Name
Esomeprazole Magnesium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 75907-119

Generic Name
Esomeprazole Magnesium
Dosage Form
Tablet, Delayed Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing

E-Z-EM Canada Inc

NDC Product
Human Prescription Drug

Varibar Thin Honey
NDC 32909-121

Generic Name
Barium Sulfate
Dosage Form
Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Varibar Honey
NDC 32909-122

Generic Name
Barium Sulfate
Dosage Form
Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Varibar Pudding
NDC 32909-125

Generic Name
Barium Sulfate
Dosage Form
Paste
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

E-z-paste
NDC 32909-770

Generic Name
Barium Sulfate
Dosage Form
Cream
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Tagitol V
NDC 32909-814

Generic Name
Barium Sulfate
Dosage Form
Suspension
Route
Oral
Marketing
NDA
Active Listing

E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Clobetasol Propionate (emollient)
NDC 0168-0301

Generic Name
Clobetasol Propionate
Dosage Form
Cream
Route
Topical
Marketing
ANDA
Active Listing

Front Line Safety

NDC Product
Human Otc Drug

First Aid Burn Cream
NDC 58228-6244

Generic Name
First Aid Burn Cream
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Genus Lifesciences Inc.

NDC Product
Human Prescription Drug

Halog
NDC 64950-126

Generic Name
Halcinonide Cream
Dosage Form
Cream
Route
Topical
Marketing
NDA
Active Listing

Glenmark Pharmaceuticals Inc., USA

NDC Product
Human Prescription Drug

Fluticasone Propionate
NDC 68462-427

Generic Name
Fluticasone Propionate
Dosage Form
Lotion
Route
Topical
Marketing
ANDA
Active Listing

H E B

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 37808-364

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Herbalife International of America, Inc.

Hikma Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Rufinamide
NDC 0054-0528

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

HyVee Inc

NDC Product
Human Otc Drug

Roll-on Pain Relief Liquid
NDC 42507-916

Generic Name
Lidocaine Hcl
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Incyte Corporation

NDC Product
Human Prescription Drug

Opzelura
NDC 50881-007

Generic Name
Ruxolitinib
Dosage Form
Cream
Route
Topical
Marketing
NDA
Active Listing

Just Brands LLC

NDC Product
Human Otc Drug

Just Cbd Soothing Unscented
NDC 73647-043

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

KROGER COMPANY

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 30142-528

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Kobayashi Healthcare International, Inc.

NDC Product
Human Otc Drug

Fungicure Night Cream
NDC 52389-681

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

Kramer Laboratories

NDC Product
Human Otc Drug

Fungi Nail Toe And Foot
NDC 55505-177

Generic Name
Tolnaftate
Dosage Form
Solution
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Fungi Nail Toe And Foot
NDC 55505-185

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

Kroger Company

NDC Product
Human Otc Drug

Kroger Lidocaine Pain Relieving
NDC 41226-740

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

Medline Industries, LP

NDC Product
Human Otc Drug

Readyprep Chg
NDC 53329-244

Generic Name
Chlorhexidine Gluconate 2%
Dosage Form
Cloth
Route
Topical
Marketing
NDA
Active Listing

NorthStar RxLLC

NDC Product
Human Prescription Drug

Atomoxetine
NDC 72603-435

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 72603-436

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 72603-437

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 72603-438

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 72603-439

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 72603-440

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 72603-441

Generic Name
Atomoxetine
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

ProStat First Aid LLC

NDC Product
Human Otc Drug

First Aid Burn Cream
NDC 58228-2044

Generic Name
First Aid Burn Cream
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

First Aid Burn Cream
NDC 58228-2309

Generic Name
First Aid Burn Cream
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

2677 First Aid Burn Cream
NDC 58228-2677

Generic Name
2677 First Aid Burn Cream
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Proper Buys LLC

PureTek Corporation

NDC Product
Human Prescription Drug

Uracin 20%
NDC 59088-257

Generic Name
Urea 20%
Dosage Form
Cream
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing

RENU LABORATORIES, LLC

NDC Product
Human Otc Drug

Impact Melanoma Spf 30
NDC 76348-598

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

Bright Guard Sport Spf
NDC 76348-675

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

Randob Labs, LTD

NDC Product
Human Otc Drug

Balmex Diaper Rash
NDC 52412-285

Generic Name
Zinc Oxide 11.3%
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Rite Aid Corporation

NDC Product
Human Otc Drug

Rite Aid Pain Relieving Roll-on
NDC 11822-9989

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

SJOLIE, INC.

NDC Product
Human Otc Drug

Sjolie Tanning Spf 30 Sunscreen
NDC 85947-001

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

Sage Products LLC

NDC Product
Human Otc Drug

Chlorhexidine Gluconate
NDC 53462-705

Generic Name
Chlorhexidine Gluconate
Dosage Form
Cloth
Route
Topical
Marketing
NDA
Active Listing

SpecGx LLC

NDC Product
Human Prescription Drug

Fentanyl Transdermal
NDC 0406-9037

Generic Name
Fentanyl Transdermal
Dosage Form
Patch, Extended Release
Route
Transdermal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fentanyl Transdermal
NDC 0406-9062

Generic Name
Fentanyl Transdermal
Dosage Form
Patch, Extended Release
Route
Transdermal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fentanyl Transdermal
NDC 0406-9100

Generic Name
Fentanyl Transdermal
Dosage Form
Patch, Extended Release
Route
Transdermal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fentanyl Transdermal
NDC 0406-9112

Generic Name
Fentanyl Transdermal
Dosage Form
Patch, Extended Release
Route
Transdermal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fentanyl Transdermal
NDC 0406-9125

Generic Name
Fentanyl Transdermal
Dosage Form
Patch, Extended Release
Route
Transdermal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fentanyl Transdermal
NDC 0406-9150

Generic Name
Fentanyl Transdermal
Dosage Form
Patch, Extended Release
Route
Transdermal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fentanyl Transdermal
NDC 0406-9175

Generic Name
Fentanyl Transdermal
Dosage Form
Patch, Extended Release
Route
Transdermal
Marketing
ANDA
Active Listing

Steel City Health Private Limited

NDC Product
Human Otc Drug

Barrier Repair Cream
NDC 85884-261

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

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Halog
NDC 10631-094

Generic Name
Halcinonide Cream
Dosage Form
Cream
Route
Topical
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Clobetasol Propionate
NDC 51672-1297

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

Halcinonide
NDC 57664-698

Generic Name
Halcinonide
Dosage Form
Cream
Route
Topical
Marketing
NDA AUTHORIZED GENERIC
Active Listing

Sunstation USA, LLC

NDC Product
Human Otc Drug

Sunstation Usa Spf-30 Sport Sunscreen-
NDC 71272-692

Generic Name
Sunstation Usa Spf-30 Sport Sunscreen-
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

TRUTEK CORP.

Tender Corporation d/b/a Adventure Ready Brands

NDC Product
Human Otc Drug

After Bite Kids
NDC 44224-1117

Generic Name
Sodium Bicarbonate
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Itch Eraser Sensitive
NDC 44224-2421

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

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Claravis
NDC 0555-1055

Generic Name
Isotretinoin
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Claravis
NDC 0555-1056

Generic Name
Isotretinoin
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Claravis
NDC 0555-1057

Generic Name
Isotretinoin
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

The J. Molner Company LLC

NDC Product
Human Prescription Drug

Clobetasol Propionate (emollient)
NDC 83148-064

Generic Name
Clobetasol Propionate
Dosage Form
Cream
Route
Topical
Marketing
ANDA
Active Listing

Veridian Healthcare

WALGREENS COMPANY

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 0363-0772

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

WESTLAKE HB PHARMA

WINCO FOODS, LLC

Walgreens

NDC Product
Human Otc Drug

Walgreen Anti-itch
NDC 0363-0263

Generic Name
Pramoxine Hcl
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 0363-1353

Generic Name
Esomeprazole Magnesium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Weeks & Leo Compnay, INC.

NDC Product
Human Otc Drug

Oxify
NDC 11383-002

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

Westlake Pharma LLC

NDC Product
Human Otc Drug

Westlake Lidocaine
NDC 82895-717

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

iON Pharma, LLC

NDC Product
Human Otc Drug

Lidosync
NDC 82944-200

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

Lidocore
NDC 82944-201

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

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