Label: ETHYL RUBBING ALCOHOL- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 15231-100-01 - Packager: COMERCIALIZADORA JIQUILPAN S.A. DE C.V.
- 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 June 5, 2011
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- ACTIVE INGREDIENT
- PURPOSE
- DOSAGE & ADMINISTRATION
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ETHYL RUBBING ALCOHOL
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:15231-100 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 29.65 mL in 100 mL DENATONIUM BENZOATE ANHYDROUS (UNII: M5BA6GAF1O) .35 mg in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:15231-100-01 500 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 02/09/1998 Labeler - COMERCIALIZADORA JIQUILPAN S.A. DE C.V. (589780068) Establishment Name Address ID/FEI Business Operations COMERCIALIZADORA JIQUILPAN S.A. DE C.V. 589780068 manufacture