Home NDC 87001-001 Antibacterial Hand Sanitizer Spray.
Product NDC 87001-001
11-digit product format 870010001
Labeler code 87001
Product ID 87001-001_446815d0-6f39-cbbe-e063-6394a90aa377
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form LIQUID
Route TOPICAL
Labeler HAIAN KANGRUI TEXTILE CO., LTD.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-08-12
Substance ALCOHOL
Active strength 62 g/112mL
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 Antibacterial Hand Sanitizer Spray.
Listing expiration 2026-12-31 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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87001-001-01 Antibacterial Hand Sanitizer Spray. 20 mL in 1 BOTTLE, SPRAY LIQUID 20 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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87001-001-01 87001000101 20 mL in 1 BOTTLE, SPRAY (87001-001-01) 20 ml 2025-08-12 No No Current