Label: 70% ISOPROPYL ALCOHOL- isopropyl alcohol liquid
- NDC Code(s): 77039-010-01
- Packager: IDO PHARM
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 30, 2025
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
For external use only
- If taken internally, serious gastric disturbances will result
- flammable, keep away from heat or flame
Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns
When using this product
- do not use in or near eyes. In case of contact with eyes, rinse eyes thoroughly with water
- do not apply over large areas of the body
- do not use longer than one week unless directed by a doctor
Stop use and ask a doctor if irritation or rash appears
Keep out of reach of children. In case of ingestion, get medical help or contact a Poison Control Center 1-800-222-1222 or dial 911 immediately
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
70% ISOPROPYL ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77039-010 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 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77039-010-01 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/12/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 01/12/2022 Labeler - IDO PHARM (694853523) Registrant - IDO PHARM (694853523) Establishment Name Address ID/FEI Business Operations IDO PHARM 694853523 manufacture(77039-010)