Home NDC 85472-004 Hand Sanitizer Mist
Product NDC 85472-004
11-digit product format 854720004
Labeler code 85472
Product ID 85472-004_3abd4d8e-0231-5e27-e063-6394a90a99cf
Type HUMAN OTC DRUG
Nonproprietary name ETHYL ALCOHOL
Dosage form SPRAY
Route TOPICAL
Labeler Zhejiang Gaorong Cosmetic Co., Ltd.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-07-25
Substance ALCOHOL
Active strength 71 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 Mist
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 71 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 85472-004-01 Hand Sanitizer Mist 35 mL in 1 BOTTLE SPRAY 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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85472-004-01 85472000401 35 mL in 1 BOTTLE (85472-004-01) 35 ml 2025-07-25 No No Current