Home NDC 73928-070 HAND SANITIZER
Product NDC 73928-070
11-digit product format 739280070
Labeler code 73928
Product ID 73928-070_36a74055-6636-0335-e063-6394a90a1568
Type HUMAN OTC DRUG
Nonproprietary name Alcohol antiseptic
Dosage form LIQUID
Route TOPICAL
Labeler Kingkey MBC Life Technology Group Co.,Ltd
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-02-01
Substance ALCOHOL
Active strength 62 mL/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 62 mL/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 73928-070-01 HAND SANITIZER 30 mL in 1 BOTTLE LIQUID 30 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 44 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 73928-070-01 73928007001 30 mL in 1 BOTTLE (73928-070-01) 30 ml 2025-02-01 No No Current