Label: HAND SANITIZER- ethanol liquid
- NDC Code(s): 69947-120-01, 69947-120-02, 69947-120-03
- Packager: Alsco Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 31, 2018
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- Drug Facts
- Active ingredient
- Purpose
- Uses
- Warnings
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
- Directions
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- Inactive ingredients
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- SPL UNCLASSIFIED SECTION
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
ethanol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69947-120 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 71 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOPROPYL ALCOHOL (UNII: ND2M416302) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL LAURATE (UNII: Y98611C087) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69947-120-01 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/03/2015 2 NDC:69947-120-02 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/03/2015 3 NDC:69947-120-03 1000 mL in 1 BAG; Type 0: Not a Combination Product 09/03/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 09/03/2015 Labeler - Alsco Inc. (007939176) Establishment Name Address ID/FEI Business Operations Best Sanitizers 627278224 manufacture(69947-120)