Label: ISOPROPYL RUBBING ALCOHOL 70%- isopropyl alcohol liquid
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NDC Code(s):
52000-010-01,
52000-010-02,
52000-010-03,
52000-010-04, view more52000-010-05, 52000-010-06, 52000-010-07
- Packager: Universal Distribution Center LLC
- 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 November 22, 2022
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- SPL UNCLASSIFIED SECTION
- INACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ISOPROPYL RUBBING ALCOHOL 70%
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52000-010 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 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:52000-010-01 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2012 2 NDC:52000-010-02 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2012 3 NDC:52000-010-03 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2012 4 NDC:52000-010-04 296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2012 5 NDC:52000-010-05 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2012 6 NDC:52000-010-06 414 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2012 7 NDC:52000-010-07 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/15/2012 Labeler - Universal Distribution Center LLC (019180459) Registrant - Universal Distribution Center LLC (019180459) Establishment Name Address ID/FEI Business Operations Anicare Pharmaceuticals Pvt. Ltd 916837425 manufacture(52000-010)