Home NDC 87858-005 Hand Sanitizer
Product NDC 87858-005
11-digit product format 878580005
Labeler code 87858
Product ID 87858-005_56cd0bb0-d3b9-ac6d-e063-6394a90af1d6
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form GEL
Route TOPICAL
Labeler NANTONG HAIYIWEI TEXTILE CO., LTD.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-16
Substance ALCOHOL
Active strength 62 g/112mL
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 62 g/112mL
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.
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 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 87858-005-01 87858000501 60 mL in 1 BOTTLE (87858-005-01) 60 ml 2026-07-16 No No Current