Hand Sanitizer

Product NDC
87001-006
11-digit product format
870010006
Labeler code
87001
Product ID
87001-006_4711fba8-4986-bf73-e063-6394a90a71bc
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 mL/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Hand Sanitizer
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL62 mL/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3K9958V90M
Rxcui1020364

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87001-006-01Hand Sanitizer35 mL in 1 BOTTLELIQUID351

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1020364ethanol 62 % Topical SprayPSN4711fb91-8afd-e5db-e063-6394a90a4b9e1
1020364ethanol 0.62 ML/ML Topical SpraySCD4711fb91-8afd-e5db-e063-6394a90a4b9e1
1020364ethanol 62 % Topical SpraySY4711fb91-8afd-e5db-e063-6394a90a4b9e1
1020364ethyl alcohol 62 % Topical SpraySY4711fb91-8afd-e5db-e063-6394a90a4b9e1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
87001-006-018700100060135 mL in 1 BOTTLE (87001-006-01) 35 ml2025-12-20NoNoHistorical