Label: ISOPROPYL ALCOHOL liquid
- NDC Code(s): 63868-153-43
- Packager: CDMA
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 April 12, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Use
- Warnings
- Flammable
- Ask a doctor
- When using this product
- Stop use
- Keep out of reach of children
- Caution
- Directions
- Other information
- Inactive ingredients
- ADVERSE REACTIONS SECTION
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principal display panel
QC
QUALITY
CHOICE
70%
Isopropyl
Alcohol
With Wintergreen
& Glycerin
First Aid Antiseptic
For Treatment of Minor
Cuts and Scranpes
WARNING
FLAMMABLE - Keep away from heat, spark, electrical, fire or flame
Use only in a well- ventiliated area: fumes can be harmful.
CAUTION: Do not point at self or others; product will squirt when squeezed.
16 fl oz ( 473 mL)

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INGREDIENTS AND APPEARANCE
ISOPROPYL ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-153 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 924 mg in 1 mL Inactive Ingredients Ingredient Name Strength FD&C BLUE NO. 1 (UNII: H3R47K3TBD) GLYCERIN (UNII: PDC6A3C0OX) METHYL SALICYLATE (UNII: LAV5U5022Y) WATER (UNII: 059QF0KO0R) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-153-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/08/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part344 03/08/2019 Labeler - CDMA (011920774) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(63868-153)
