Label: ISOPROPYL RUBBING ALCOHOL 70- isopropyl alcohol solution
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NDC Code(s):
61734-012-01,
61734-012-02,
61734-012-03,
61734-012-04, view more61734-012-05, 61734-012-06, 61734-012-07, 61734-012-08, 61734-012-09, 61734-012-10
- Packager: Delon Laboratories (1990) Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 30, 2024
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- Active ingredient
- Purpose
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- Warnings
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- Inactive ingredient
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ISOPROPYL RUBBING ALCOHOL 70
isopropyl alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61734-012 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:61734-012-01 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/04/2014 2 NDC:61734-012-02 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/04/2014 12/04/2014 3 NDC:61734-012-03 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/04/2014 12/04/2014 4 NDC:61734-012-04 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/04/2014 12/04/2014 5 NDC:61734-012-05 3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/04/2014 12/04/2014 6 NDC:61734-012-06 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 10/04/2014 10/20/2022 7 NDC:61734-012-07 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/04/2014 12/04/2014 8 NDC:61734-012-08 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/04/2014 12/04/2014 9 NDC:61734-012-09 174 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 10/04/2014 10/31/2019 10 NDC:61734-012-10 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/27/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 05/07/2010 Labeler - Delon Laboratories (1990) Ltd. (248364184) Establishment Name Address ID/FEI Business Operations Laboratoires Delon 208896216 label(61734-012) , manufacture(61734-012) , pack(61734-012)