Label: ANTIBACTERIAL HAND SANITIZER- ethyl alcohol gel
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NDC Code(s):
71513-105-01,
71513-105-03,
71513-105-04,
71513-105-05, view more71513-105-06, 71513-105-50
- Packager: Broder Bros Co.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 28, 2023
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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL HAND SANITIZER
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71513-105 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71513-105-01 29.57 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2021 2 NDC:71513-105-03 59.12 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2021 02/28/2026 3 NDC:71513-105-04 236.59 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2021 02/28/2026 4 NDC:71513-105-05 473.18 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2021 02/28/2026 5 NDC:71513-105-06 14.79 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2021 02/28/2026 6 NDC:71513-105-50 29.57 mL in 1 TUBE; Type 0: Not a Combination Product 01/01/2021 02/28/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/01/2021 Labeler - Broder Bros Co. (107044246)