Label: ANTIBACTERIAL HAND SANITIZER- alcohol spray
- NDC Code(s): 71160-189-05, 71160-189-10, 71160-189-20, 71160-189-25
- Packager: TEKWELD SOLUTIONS, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 5, 2024
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- Drug Facts
- Active Ingredients
- Uses:
- Warnings:
- Directions:
- Other Information:
- Inactive Ingredients:
- Questions or Comments?
- Package Labeling:71160-189-05
- Package Labeling:71160-189-10
- Package Labeling: 70412-189-20
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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL HAND SANITIZER
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71160-189 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 620 mg in 1 mL Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71160-189-10 10 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/09/2017 2 NDC:71160-189-05 5 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/09/2017 3 NDC:71160-189-25 25 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/09/2017 4 NDC:71160-189-20 20 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/09/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/09/2017 Labeler - TEKWELD SOLUTIONS, INC. (169803389)