Label: 70%- isopropyl alcohol liquid
- NDC Code(s): 50804-810-08, 50804-810-43, 50804-810-45, 50804-810-72
- Packager: Perrigo Direct, 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 October 27, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Flammable
- Ask a Doctor before use
- When using theis product
- Stop use and ask a doctor
- Keep out of reach of children
- Caution
- Directions
- Other information
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
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principal display panel
NDC 50804-810-43
GoodSense
70% Isopropyl Alcohol
- First Aid Antisetpic
- For Rubbing and Massaging
WARNING FLAMMABLE Keep away 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 squeezed.
16FL OZ (1PT) 473mL
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INGREDIENTS AND APPEARANCE
70%
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50804-810 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:50804-810-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/08/2010 2 NDC:50804-810-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/08/2010 3 NDC:50804-810-72 295 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/08/2010 4 NDC:50804-810-08 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/08/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/08/2010 Labeler - Perrigo Direct, Inc. (076059836) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(50804-810) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(50804-810)