Label: ISOPROPYL ALCOHOL liquid
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NDC Code(s):
10565-071-04,
10565-071-08,
10565-071-16,
10565-071-32, view more10565-071-99
- Packager: Hydrox Laboratories
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 26, 2023
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredient
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ISOPROPYL ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10565-071 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 91 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:10565-071-04 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/05/2019 2 NDC:10565-071-08 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/05/2019 3 NDC:10565-071-32 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/26/2017 4 NDC:10565-071-16 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/26/2017 5 NDC:10565-071-99 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/26/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 05/19/2017 Labeler - Hydrox Laboratories (025164302) Registrant - Hydrox Laboratories (025164302) Establishment Name Address ID/FEI Business Operations Hydrox Laboratories 025164302 manufacture(10565-071) , label(10565-071) , pack(10565-071)