Home NDC 87374-003-01 Hand sanitizer
Product NDC 87374-003
Requested package NDC 87374-003-01
11-digit product format 873740003
Labeler code 87374
Product ID 87374-003_56a22363-f532-d9bd-e063-6294a90a020b
Type HUMAN OTC DRUG
Nonproprietary name Hand sanitizer spray
Dosage form SPRAY
Route TOPICAL
Labeler Beimei Biotechnology (Guangzhou) Co., Ltd.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-15
Substance ALCOHOL
Active strength 70 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 70 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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1041849 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 100 of 114 · 2,277 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87374-003-01 87374000301 30 mL in 1 BOTTLE, SPRAY (87374-003-01) 30 ml 2026-07-15 No No Current