Label: 50% RUBBING- isopropyl alcohol liquid
- NDC Code(s): 0869-0864-18, 0869-0864-43, 0869-0864-72
- Packager: Vi-Jon, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 1, 2023
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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
- keep out of children
- SPL UNCLASSIFIED SECTION
- Directions
- Other Information
- Inactive ingredient
- Adverse reactions
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principal display panel
NDC 0869-0864-43
swan
50% Isopropyl Alcohol
- First Aid Antiseptic
- For Rubbing & Massaging
Square bottle uses less plastic then a similarly sized round 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 others; product will squirt when squeezed.
Use only in a well-ventilated area; fumes can be harmful
16 FL OZ (1PT) (473 mL)
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principal display panel
mountain
falls
body
rub
topical antiseptic
& sanitizer
for treatment of minor cuts and scrapes
50%
isopropyl alcohol
first aid antiseptic
WARNING FLAMMABLE - Keep aeay from heat, spark, electrical, fire or flame
Use only in a well-ventilated area: fumes can be harmful
Caution: Do not point at self or others; product will squirt when squeeed.
10 FL OZ (295 mL)
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INGREDIENTS AND APPEARANCE
50% RUBBING
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0869-0864 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 50 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:0869-0864-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/1989 2 NDC:0869-0864-18 118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/15/1989 3 NDC:0869-0864-72 295 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/15/1989 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/15/1989 Labeler - Vi-Jon, LLC (790752542) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(0869-0864) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(0869-0864)