Label: ISOPROPYL ALCOHOL liquid
- NDC Code(s): 72288-904-43, 72288-904-45, 72288-904-72
- Packager: Amazon.Com Services LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 28, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- Flammable
- Ask a doctor before use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Caution
- Directions
- Other information
- Inactive ingredient
- SPL UNCLASSIFIED SECTION
- Principal display panel
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INGREDIENTS AND APPEARANCE
ISOPROPYL ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72288-904 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.91 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72288-904-72 295 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 05/01/2018 2 NDC:72288-904-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/01/2018 3 NDC:72288-904-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 05/01/2018 Labeler - Amazon.Com Services LLC (128990418) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(72288-904) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(72288-904)