Label: ETHYL ALCOHOL gel
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Contains inactivated NDC Code(s)
NDC Code(s): 49283-700-64 - Packager: Chemco Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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Drug Label Information
Updated September 8, 2020
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- DOSAGE & ADMINISTRATION
- WARNINGS
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
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- PURPOSE
- ACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
ETHYL ALCOHOL
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49283-700 Route of Administration TOPICAL 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 .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69) ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 20 (UNII: 7T1F30V5YH) CARBOMER 940 (UNII: 4Q93RCW27E) TROLAMINE (UNII: 9O3K93S3TK) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) BENZYL SALICYLATE (UNII: WAO5MNK9TU) LINALOOL, (+/-)- (UNII: D81QY6I88E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49283-700-64 1892 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/08/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/08/2020 Labeler - Chemco Corporation (032495954) Registrant - Chemco Corporation (032495954) Establishment Name Address ID/FEI Business Operations Chemco Corporation 032495954 manufacture(49283-700)