Label: HAND SANITIZER- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 19392-130-01 - Packager: Bullet Line, LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated December 17, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- INACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:19392-130 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 630 mL in 1000 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) BITTER ORANGE OIL (UNII: 9TLV70SV6I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:19392-130-01 8 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/08/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 10/08/2014 Labeler - Bullet Line, LLC (122539042)