Label: HAND SANITIZER- ethanol liquid
- NDC Code(s): 70124-110-02, 70124-110-03
- Packager: Sloan Valve Company
- 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 October 17, 2015
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- Drug Facts
- Active ingredients
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- KEEP OUT OF REACH OF CHILDREN
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
ethanol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70124-110 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:70124-110-02 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/20/2015 2 NDC:70124-110-03 1000 mL in 1 BAG; Type 0: Not a Combination Product 07/20/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 07/20/2015 Labeler - Sloan Valve Company (005121033) Establishment Name Address ID/FEI Business Operations Best Sanitizers, Inc 627278224 manufacture(70124-110)