Home NDC 85279-003 HAND SANITIZER
Product NDC 85279-003
11-digit product format 852790003
Labeler code 85279
Product ID 85279-003_487b2cdf-8ef7-0436-e063-6394a90ac44c
Type HUMAN OTC DRUG
Nonproprietary name HAND SANITIZER
Dosage form LIQUID
Route TOPICAL
Labeler Guangdong bangze medicine co., ltd
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-08-06
Substance ALCOHOL
Active strength 62 g/100mL
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 HAND SANITIZER
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 62 g/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 SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85279-003-01 HAND SANITIZER 30 mL in 1 BOTTLE LIQUID 30 3 85279-003-02 HAND SANITIZER 35 mL in 1 BOTTLE LIQUID 35 3
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 85279-003-01 85279000301 30 mL in 1 BOTTLE (85279-003-01) 30 ml 2025-08-06 No No Current 85279-003-02 85279000302 35 mL in 1 BOTTLE (85279-003-02) 35 ml 2025-08-06 No No Current