HAND SANTIZER- alcohol liquid
Hand Santizer by
Drug Labeling and Warnings
Hand Santizer by is a Otc medication manufactured, distributed, or labeled by Robert Mazza, Inc dba Five & 20 Spirits, Robert Mazza, Inc.. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- WARNINGS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HAND SANTIZER
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 74054-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) HYDROGEN PEROXIDE (UNII: BBX060AN9V) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 74054-100-02 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/26/2020 2 NDC: 74054-100-03 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/26/2020 3 NDC: 74054-100-04 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/26/2020 4 NDC: 74054-100-05 18927 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/26/2020 5 NDC: 74054-100-06 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/26/2020 6 NDC: 74054-100-07 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/26/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/26/2020 Labeler - Robert Mazza, Inc dba Five & 20 Spirits (114974231) Registrant - Robert Mazza, Inc. (114974231) Establishment Name Address ID/FEI Business Operations Robert Mazza, Inc. 114974231 manufacture(74054-100)
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