NDC 61924-102

HAND-E-FOAM

Otc Antimicrobial Drug Products

HAND-E-FOAM is a Topical Aerosol, Foam in the Human Otc Drug category. It is labeled and distributed by Dermarite Industries, Llc. The primary component is Benzethonium Chloride.

Product ID61924-102_777faa78-a73f-1236-e053-2a91aa0ac3ec
NDC61924-102
Product TypeHuman Otc Drug
Proprietary NameHAND-E-FOAM
Generic NameOtc Antimicrobial Drug Products
Dosage FormAerosol, Foam
Route of AdministrationTOPICAL
Marketing Start Date2002-08-08
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameDermaRite Industries, LLC
Substance NameBENZETHONIUM CHLORIDE
Active Ingredient Strength0 g/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 61924-102-08

237 mL in 1 BOTTLE, PUMP (61924-102-08)
Marketing Start Date2002-08-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 61924-102-34 [61924010234]

HAND-E-FOAM AEROSOL, FOAM
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2002-08-08

NDC 61924-102-08 [61924010208]

HAND-E-FOAM AEROSOL, FOAM
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2002-08-08

NDC 61924-102-17 [61924010217]

HAND-E-FOAM AEROSOL, FOAM
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2002-08-08

Drug Details

Active Ingredients

IngredientStrength
BENZETHONIUM CHLORIDE.002 g/mL

OpenFDA Data

SPL SET ID:00d2afd0-58b5-4aba-a762-d10ef1bc3f58
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1041869
  • UPC Code
  • 0714196108081
  • NDC Crossover Matching brand name "HAND-E-FOAM" or generic name "Otc Antimicrobial Drug Products"

    NDCBrand NameGeneric Name
    61924-102HAND-E-FOAMOTC ANTIMICROBIAL DRUG PRODUCTS
    61924-107SAN-E-FOAMOTC ANTIMICROBIAL DRUG PRODUCTS

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