Home NDC 77665-105 Hand sanitizer
Product NDC 77665-105
11-digit product format 776650105
Labeler code 77665
Product ID 77665-105_45f542d1-3afb-3f2c-e063-6294a90a2d62
Type HUMAN OTC DRUG
Nonproprietary name hand sanitizer spray
Dosage form SPRAY
Route TOPICAL
Labeler Guangzhou Baihua Co., Ltd
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-07-24
Substance ALCOHOL
Active strength 70 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
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 2026-12-31 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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 77665-105-01 Hand sanitizer 30 mL in 1 BOTTLE SPRAY 30 2
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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 77665-105-01 77665010501 30 mL in 1 BOTTLE (77665-105-01) 30 ml 2025-07-24 No No Current