Label: ISOPROPYL ALCOHOL liquid
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NDC Code(s):
0869-0810-08,
0869-0810-43,
0869-0810-45,
0869-0810-72, view more0869-0810-99
- Packager: Vi-Jon, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated April 26, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- 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
- Adverse reaction
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principal display panel
NDC 0869-0810-45
SWAN
70% Isopropyl Alcohol
- First Aid Antseptic
- For Rubbing & Massaging
Square bottle uses less plastic than a similarly sized bottle Recyclable (if available in your area)
WARNING FLAMMABLE-Keep away from heat, spark, electrical fire or flame
CAUTION: Do not point at self or other; product will squirt when squeezed.
Use only in a well-ventilated area: fumes can be harmful
32 FL OZ (1 QT) 946 mL
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INGREDIENTS AND APPEARANCE
ISOPROPYL ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0869-0810 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0869-0810-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/1989 2 NDC:0869-0810-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/1989 3 NDC:0869-0810-08 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/1989 4 NDC:0869-0810-99 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/1989 04/26/2024 5 NDC:0869-0810-72 295 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/09/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 07/15/1989 Labeler - Vi-Jon, LLC (088520668) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(0869-0810)