Label: HAND SANITIZER- alcohol liquid
- NDC Code(s): 75214-502-12, 75214-502-50
- Packager: HANUL CO.,LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 9, 2024
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- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75214-502 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 1.45 mL in 100 mL HYDROGEN PEROXIDE (UNII: BBX060AN9V) 0.12 mL in 100 mL WATER (UNII: 059QF0KO0R) 17.68 mL in 100 mL CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E) 0.4 mL in 100 mL AMINOMETHYLPROPANOL (UNII: LU49E6626Q) 0.3 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75214-502-50 500 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 03/30/2020 2 NDC:75214-502-12 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 03/30/2020 Labeler - HANUL CO.,LTD (557814370) Establishment Name Address ID/FEI Business Operations HANUL CO.,LTD 557814370 manufacture(75214-502)