Label: ISOPROPYL ALCOHOL liquid
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NDC Code(s):
59779-804-38,
59779-804-43,
59779-804-45,
59779-804-72, view more59779-804-99
- Packager: CVS Pharmacy, Inc
- 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 September 27, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- 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 ingredients
- SPL UNCLASSIFIED SECTION
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principal display panel
CVSHealth
Isopropyl Alcohol
FIRST AID ANTISEPTIC
For treatment of minor cuts and scrapes
91%
Caution: Do not point at self or others; product wil squirt when squeezed.
Use only in a well-ventilated area; fumes can be harmful
WARNING FLAMABLE Keep away from heat, spark, electrical, fire or flame
10 FL OZ (296 mL)
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INGREDIENTS AND APPEARANCE
ISOPROPYL ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-804 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL .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:59779-804-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/1992 2 NDC:59779-804-99 296 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/15/1992 3 NDC:59779-804-45 946 mL in 1 PACKAGE; Type 0: Not a Combination Product 07/15/1992 4 NDC:59779-804-38 295 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/1992 5 NDC:59779-804-72 296 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/15/1992 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/15/1992 Labeler - CVS Pharmacy, Inc (062312574) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(59779-804) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(59779-804)