Home NDC 59448-008 Instant Hand Antiseptic
Product NDC 59448-008
11-digit product format 594480008
Labeler code 59448
Product ID 59448-008_dcc29c32-04fb-49c5-8ce3-7bc2cdff346a
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form GEL
Route TOPICAL
Labeler ASP Global
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-10-01
Substance ALCOHOL
Active strength 62 mL/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Instant Hand Antiseptic
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 62 mL/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3K9958V90M Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 581660 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59448-008-01 Wellstar Amenity 53 mL in 1 BOTTLE, PLASTIC GEL 53 mL 62 mL in 100mL 4 59448-008-01 Instant Hand Antiseptic 53 mL in 1 BOTTLE, PLASTIC GEL 53 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59448-008 WELLSTAR AMENITY (BENZALKONIUM CHLORIDE AND SODIUM MONOFLUOROPHOSPHATE ) KIT [ASP GLOBAL, LLC] 4 Current NDC, Legacy NDC 20241222_ced9dd96-7922-43d7-906f-32afaad733ec.zip 59448-008 INSTANT HAND ANTISEPTIC (ALCOHOL) GEL [ASP GLOBAL] 2 Current NDC, Legacy NDC, 1 package rows 20241208_9aca3f89-cdde-430c-8eb6-43a3ac3fc0df.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 100 of 115 · 2,286 matching rows.
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 59448-008-01 59448000801 53 mL in 1 BOTTLE, PLASTIC (59448-008-01) 53 ml 2021-10-01 0000-00-00 No No Current