Home NDC 61924-093-34 KLEENFOAM
Product NDC 61924-093
Requested package NDC 61924-093-34
11-digit product format 619240093
Labeler code 61924
Product ID 61924-093_9c5944f3-939d-b174-e053-2995a90ac030
Type HUMAN OTC DRUG
Nonproprietary name OTC ANTIMICROBIAL DRUG PRODUCT
Dosage form AEROSOL, FOAM
Route TOPICAL
Labeler Dermarite Industries LLC
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2011-12-12
Marketing end 0000-00-00
Substance CHLOROXYLENOL
Active strength 0 g/mL
NDC exclude flag No
Listing certified through 2021-12-31
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 · 9 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…2022-08-30 03:57 UTC · source 2022-08-29 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 61924-093-34 KLEENFOAM 1000 mL in 1 CARTRIDGE AEROSOL, FOAM 1000 7
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Chloroxylenol ACTIVE INGREDIENT 0F32U78V2Q KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 CHLOROXYLENOL ACTIVE MOIETY 0F32U78V2Q KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 ALOE VERA LEAF INACTIVE INGREDIENT ZY81Z83H0X KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 CITRIC ACID MONOHYDRATE INACTIVE INGREDIENT 2968PHW8QP KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 Cocamidopropyl Betaine INACTIVE INGREDIENT 5OCF3O11KX KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 COCO MONOETHANOLAMIDE INACTIVE INGREDIENT C80684146D KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 DMDM Hydantoin INACTIVE INGREDIENT BYR0546TOW KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 EDETATE SODIUM INACTIVE INGREDIENT MP1J8420LU KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 LEMON OIL INACTIVE INGREDIENT I9GRO824LL KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 Methylchloroisothiazolinone INACTIVE INGREDIENT DEL7T5QRPN KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 Methylisothiazolinone INACTIVE INGREDIENT 229D0E1QFA KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 POLYSORBATE 20 INACTIVE INGREDIENT 7T1F30V5YH KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 Propylene Glycol INACTIVE INGREDIENT 6DC9Q167V3 KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 Sodium Chloride INACTIVE INGREDIENT 451W47IQ8X KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 Sodium Hydroxide INACTIVE INGREDIENT 55X04QC32I KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 SODIUM ISOSTEAROYL LACTYLATE INACTIVE INGREDIENT 8730J0D3EV KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 Sodium Laureth Sulfate INACTIVE INGREDIENT BPV390UAP0 KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 Sodium Lauryl Sulfate INACTIVE INGREDIENT 368GB5141J KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3 WATER INACTIVE INGREDIENT 059QF0KO0R KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61924-093 KLEENFOAM (OTC ANTIMICROBIAL DRUG PRODUCT) AEROSOL, FOAM [DERMARITE INDUSTRIES LLC] 7 Legacy NDC, 1 package rows 20241208_f4ea9ae8-c783-48b4-af31-a26ecaa34992.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 61924-093-34 61924009334 1000 mL in 1 CARTRIDGE (61924-093-34) 1000 ml 2011-12-12 0000-00-00 No No Current