Label: ISOPROPYL ALCOHOL liquid
- NDC Code(s): 67326-035-00
- Packager: Degasa, S.A. de C.V.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 5, 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
- Inactive Ingredients
- Uses
-
Warnings
For external use onlyFlammable
- Keep away from fire or flame, heat, spark, electrical
When using this product
- Do not get into eyes
- Do not inhale
- Do not apply over large areas of the body
- Do not use longer than 1 week
- Directions
- Other Information
- Question or comments?
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
ISOPROPYL ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67326-035 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.91 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67326-035-00 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/20/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 10/20/2020 Labeler - Degasa, S.A. de C.V. (812771980) Establishment Name Address ID/FEI Business Operations Degasa, S.A. de C.V. 812771980 manufacture(67326-035)