Home NDC 21749-808-51 PURELL Advanced Hand Sanitizer Green Certified Foam
Product NDC 21749-808
Requested package NDC 21749-808-51
11-digit product format 217490808
Labeler code 21749
Product ID 21749-808_57d91ee6-a167-dc13-e063-6294a90a2f5e
Type HUMAN OTC DRUG
Nonproprietary name alcohol
Dosage form LIQUID
Route TOPICAL
Labeler GOJO Industries, LLC
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-31
Substance ALCOHOL
Active strength .7 mL/mL
NDC exclude flag No
Listing certified through 2027-12-31
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 PURELL Advanced Hand Sanitizer Green Certified Foam
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL .7 mL/mL
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 616805 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 21749-808-51 21749080851 550 mL in 1 BOTTLE (21749-808-51) 550 ml 2026-07-31 No No Current