- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- ACTIVE INGREDIENT
- WARNINGS
- INDICATIONS & USAGE
- PURPOSE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ISOPROPYL ALCOHOL 99%
isopropyl alcohol 99% liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70677-0045 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 990 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 1 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70677-0045-1 473 mL in 1 CONTAINER; Type 0: Not a Combination Product 07/01/2018 05/31/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/01/2018 05/31/2022 Labeler - Strategic Sourcing Services LLC (116956644) Registrant - Humco Holding Group, Inc. (825672884) Establishment Name Address ID/FEI Business Operations Humco Holding Group, Inc. 825672884 manufacture(70677-0045) , pack(70677-0045)