Home NDC 56136-021 Foaming Mousse Anti-Bacterial Hand Sanitizer
Product NDC 56136-021
11-digit product format 561360021
Labeler code 56136
Product ID 56136-021_7ed0bf57-ddd2-4864-a95f-f0dd7fa0b511
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form AEROSOL, FOAM
Route TOPICAL
Labeler Ganzhou Olivee Cosmetic Co., Ltd.
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2018-11-28
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 Foaming Mousse Anti-Bacterial Hand Sanitizer
Brand name suffix Cherry Scented
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 616763 Internal RxNorm 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 56136-021-01 Foaming Mousse Anti-Bacterial Hand SanitizerCherry Scented 50 mL in 1 BOTTLE AEROSOL, FOAM 50 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 56136-021 FOAMING MOUSSE ANTI-BACTERIAL HAND SANITIZER CHERRY SCENTED (ALCOHOL) AEROSOL, FOAM [GANZHOU OLIVEE COSMETIC CO., LTD.] 1 Current NDC, Legacy NDC, 1 package rows 20181201_35bd0f8f-1602-4713-b20f-8dc38e2761c2.zip
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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 56136-021-01 56136002101 50 mL in 1 BOTTLE (56136-021-01) 50 ml 2018-11-28 0000-00-00 No No Current