Label: HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 79352-001-01, 79352-001-02, 79352-001-03, 79352-001-04, view more79352-001-05, 79352-001-06 - Packager: AEROQUEST, INC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated June 23, 2020
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- Active Ingredient
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- Directions
- Inactive ingredients
- Product Label
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79352-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) TERT-BUTYL ALCOHOL (UNII: MD83SFE959) DENATONIUM BENZOATE ANHYDROUS (UNII: M5BA6GAF1O) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79352-001-01 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/01/2020 2 NDC:79352-001-02 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/01/2020 3 NDC:79352-001-03 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/01/2020 4 NDC:79352-001-04 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/01/2020 5 NDC:79352-001-05 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/01/2020 6 NDC:79352-001-06 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/01/2020 Labeler - AEROQUEST, INC (883142077)