Label: ISOPROPYL ALCOHOL spray
- NDC Code(s): 69103-5500-0
- Packager: Provision Medical
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 14, 2024
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- Active Ingredients
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- Inactive Ingredients
- Principal Display Panel – 2 fl. oz Bottle Label
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INGREDIENTS AND APPEARANCE
ISOPROPYL ALCOHOL
isopropyl alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69103-5500 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 700 mL in 1 L Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69103-5500-0 0.0591 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/25/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 07/25/2022 Labeler - Provision Medical (036936831) Registrant - : Safetec of America, Inc. (874965262) Establishment Name Address ID/FEI Business Operations Safetec of America, Inc. 874965262 manufacture(69103-5500)