Label: 50% ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 18027-002-01, 18027-002-02, 18027-002-03, 18027-002-04, view more18027-002-05, 18027-002-06, 18027-002-07 - Packager: AMERICAN CONSUMER PRODUCTS LLC
- Category: HUMAN OTC DRUG LABEL
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 July 20, 2017
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- Official Label (Printer Friendly)
- 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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
50% ISOPROPYL RUBBING ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:18027-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 50 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:18027-002-01 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/2017 2 NDC:18027-002-02 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/2017 3 NDC:18027-002-03 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/2017 4 NDC:18027-002-04 296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/2017 5 NDC:18027-002-05 354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/2017 6 NDC:18027-002-06 414 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/2017 7 NDC:18027-002-07 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/15/2017 Labeler - AMERICAN CONSUMER PRODUCTS LLC (858427334) Registrant - Anicare Pharmaceuticals Pvt. Ltd (916837425) Establishment Name Address ID/FEI Business Operations Anicare Pharmaceuticals Pvt. Ltd 916837425 manufacture(18027-002)
