Label: ISOPROPYL ALCOHOL liquid
- NDC Code(s): 37808-804-43, 37808-804-45, 37808-804-72
- Packager: H-E-B
- Category: HUMAN OTC DRUG LABEL
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 January 9, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- purpose
- Use
- 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 ingredients
- Adverse Reaction
-
principal display panel
H-E-B
91% Isopropyl Alcohol
First Aid Antiseptic
- Decreases Germs in Minor Cuts and Scrapes
WARNING FLAMMABLE - Keep away from heat, spark, electrical, fire or flame
CAUTON: Do not point at self or others when squeezed
Use only in a well-ventilated area: fumes an be harmful
CAUTON: Do not point at self or others when squeezed
H-E-B
100% Guarantee promise
If you arn't completely pleased with this product, we will be happy to replace it or refund your money.
You have our word on it
32 FL OZ (1QT) 946mL
-
INGREDIENTS AND APPEARANCE
ISOPROPYL ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-804 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 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:37808-804-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/13/2015 2 NDC:37808-804-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/13/2015 3 NDC:37808-804-72 295 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/13/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/13/2015 Labeler - H-E-B (007924756) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(37808-804) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(37808-804)