Home NDC 87660-105 Hand Sanitizer
Product NDC 87660-105
11-digit product format 876600105
Labeler code 87660
Product ID 87660-105_525198e3-a0b3-6988-e063-6294a90aa634
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Guangdong Yanze Biotechnology Co., Ltd.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-18
Substance ALCOHOL
Active strength 6.2 mL/10mL
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 6.2 mL/10mL
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 1020364 Internal RxNorm 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 87660-105-01 Hand Sanitizer 35 mL in 1 BOTTLE LIQUID 35 1
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 91 of 114 · 2,275 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87660-105-01 87660010501 35 mL in 1 BOTTLE (87660-105-01) 35 ml 2026-05-18 No No Current