Home NDC 87910-005-01 Hydrating Hand Sanitizer ALOE BREEZE
Product NDC 87910-005
Requested package NDC 87910-005-01
11-digit product format 879100005
Labeler code 87910
Product ID 87910-005_585e6406-8d55-2c50-e063-6394a90ab0a6
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL 75%
Dosage form LIQUID
Route TOPICAL
Labeler Guangzhou Ailizhuangsi Cosmetics Co., Ltd.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-06
Substance ALCOHOL
Active strength .75 g/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 Hydrating Hand Sanitizer ALOE BREEZE
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL .75 g/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 2286295 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 9 of 115 · 2,286 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87910-005-01 87910000501 30 mL in 1 BOTTLE (87910-005-01) 30 ml 2026-08-06 No No Current