Label: 70% ISOPROPYL ALCOHOL- isopropyl alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 79590-002-00 - Packager: MBS Medical Technologies Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 September 15, 2020
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- active ingredient
- purpose
- use
- warnings
- ask a doctor
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- caution
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- Other information
- inactive ingredients
- SPL UNCLASSIFIED SECTION
- principal display panel
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INGREDIENTS AND APPEARANCE
70% ISOPROPYL ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79590-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 700 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79590-002-00 475 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/15/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/15/2020 Labeler - MBS Medical Technologies Inc (117581535) Registrant - MBS Medical Technologies Inc (117581535) Establishment Name Address ID/FEI Business Operations MBS Medical Technologies Inc 117581535 manufacture(79590-002)