Home NDC 87858-002 Hand Sanitizer
Product NDC 87858-002
11-digit product format 878580002
Labeler code 87858
Product ID 87858-002_56ca837d-d061-fb94-e063-6294a90ac9da
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form SPRAY
Route TOPICAL
Labeler NANTONG HAIYIWEI TEXTILE CO., LTD.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-16
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.
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 100 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 87858-002-01 87858000201 35 mL in 1 BOTTLE (87858-002-01) 35 ml 2026-07-16 No No Current