Label: ALCOHOL- isopropyl alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 61767-305-01 - Packager: Blossom Pharmaceuticals
- 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 January 31, 2014
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
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WARNINGS
- For external use only
- Flammable, keep away from fire or flame, heat, spark, electrical.
- Not for use with electrocautinary devices or procedures
- Ask a doctor before use if you have deep puncture wounds, animal bites or serious burns.
- Stop use and ask a doctor if condition persist or gets worse.
For rubbing and massaging:
- Caution: Do not apply to irritated skinor if excessive irritation develops
- Avoid getting into eyes or mucous membranes
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER INFORMATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61767-305 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.99 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61767-305-01 473 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/29/2014 Labeler - Blossom Pharmaceuticals (677381470) Establishment Name Address ID/FEI Business Operations Blossom Pharmaceuticals 677381470 manufacture(61767-305)