Home NDC 61924-102-34 HAND-E-FOAM
Product NDC 61924-102
Requested package NDC 61924-102-34
11-digit product format 619240102
Labeler code 61924
Product ID 61924-102_efd152e8-8c38-5fad-e053-2995a90a2297
Type HUMAN OTC DRUG
Nonproprietary name OTC ANTIMICROBIAL DRUG PRODUCTS
Dosage form AEROSOL, FOAM
Route TOPICAL
Labeler DermaRite Industries, LLC
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2002-08-08
Marketing end 0000-00-00
Substance BENZETHONIUM CHLORIDE
Active strength 0 g/mL
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 61924-102-08 HAND-E-FOAM 237 mL in 1 BOTTLE, PUMP AEROSOL, FOAM 237 8 61924-102-17 HAND-E-FOAM 50 mL in 1 BOTTLE, PUMP AEROSOL, FOAM 50 8 61924-102-34 HAND-E-FOAM 1000 mL in 1 CARTRIDGE AEROSOL, FOAM 1000 8
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Benzethonium Chloride ACTIVE INGREDIENT PH41D05744 HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 BENZETHONIUM ACTIVE MOIETY 1VU15B70BP HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 .ALPHA.-TOCOPHEROL ACETATE INACTIVE INGREDIENT 9E8X80D2L0 HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 Benzalkonium Chloride INACTIVE INGREDIENT F5UM2KM3W7 HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 Cetrimonium Chloride INACTIVE INGREDIENT UC9PE95IBP HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 Diazolidinyl Urea INACTIVE INGREDIENT H5RIZ3MPW4 HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 Glycerin INACTIVE INGREDIENT PDC6A3C0OX HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 Hydroxyethyl Cetyldimonium Phosphate INACTIVE INGREDIENT 9G05UO431K HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 METHYLCHLOROISOTHIAZOLINONE INACTIVE INGREDIENT DEL7T5QRPN HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 METHYLISOTHIAZOLINONE INACTIVE INGREDIENT 229D0E1QFA HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 Methylparaben INACTIVE INGREDIENT A2I8C7HI9T HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 PEG-8 DIMETHICONE INACTIVE INGREDIENT GIA7T764OD HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 PEG-8 Ricinoleate INACTIVE INGREDIENT DM36F4D2OU HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 POLYOXYL 40 HYDROGENATED CASTOR OIL INACTIVE INGREDIENT 7YC686GQ8F HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 Propylene Glycol INACTIVE INGREDIENT 6DC9Q167V3 HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 Propylparaben INACTIVE INGREDIENT Z8IX2SC1OH HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 Sodium Hydroxide INACTIVE INGREDIENT 55X04QC32I HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2 Water INACTIVE INGREDIENT 059QF0KO0R HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61924-102 HAND-E-FOAM (OTC ANTIMICROBIAL DRUG PRODUCTS) AEROSOL, FOAM [DERMARITE INDUSTRIES, LLC] 8 Legacy NDC, 3 package rows 20241208_00d2afd0-58b5-4aba-a762-d10ef1bc3f58.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 61924-102-34 61924010234 1000 mL in 1 CARTRIDGE (61924-102-34) 1000 ml 2002-08-08 0000-00-00 No No Current