Label: ISOPROPYL ALCOHOL 70 PERCENT- isopropyl alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 10135-106-08, 10135-106-18 - Packager: Marlex Pharmaceuticals Inc
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated August 1, 2015
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Ask a doctor before use if you have
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
ISOPROPYL ALCOHOL 70 PERCENT
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10135-106 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:10135-106-08 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:10135-106-18 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333A 08/01/2015 Labeler - Marlex Pharmaceuticals Inc (782540215)