Label: ODORONO ANTIPERSPIRANT AND DEODORANT ROLL-ON POWDER- aluminum chlorohydrate liquid
- NDC Code(s): 51048-202-25
- Packager: Omega & Delta Co
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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Drug Label Information
Updated November 12, 2020
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SPL UNCLASSIFIED SECTION
24 HORAS DE PROTECCIÓN !Odorono, Sí Responde!
USO: Reduce la humedad en las axilas. PRECAUCIONES: Solo para uso externo. No usar sobre piel irritada o lastimada. Detenga su uso si presenta irritación o alguna molestia. Mantengase fuera del alcance de los niños. Si se ingiere buscar ayuda médica. INSTRUCCIONES DE USO: Aplique unicamente en las axilas. INGREDIENTE ACTIVO: Clorohidrato de aluminio OTROS INGREDIENTES: Agua, PPG-15 estearil éter, Estearet-2, Estearet-21, Fragancia, EDTA disódico, BHT, Triclosán. IMPORTADO Y DISTRIBUIDO POR:El Salvador - Dizac S.A. de C.V., Registro No. 1EC94191208 Panamá - Medimex S.A., Registro No. 64611 Nicaragua - Contesa S.A., Registro No. México - Grupo Agroindustrial San Miguel, Candido Aviles #37 Col. Lomas de Memetla Distrito Federal, C.P. 05330 R.F.C. GAS960629976. - SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- STOP USE
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ODORONO ANTIPERSPIRANT AND DEODORANT ROLL-ON POWDER
aluminum chlorohydrate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51048-202 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE 20 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PPG-15 STEARYL ETHER (UNII: 1II18XLS1L) STEARETH-2 (UNII: V56DFE46J5) STEARETH-21 (UNII: 53J3F32P58) EDETATE DISODIUM (UNII: 7FLD91C86K) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) TRICLOSAN (UNII: 4NM5039Y5X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51048-202-25 74 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 05/08/2006 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 05/08/2006 Labeler - Omega & Delta Co (090317793) Establishment Name Address ID/FEI Business Operations Omega & Delta Co 090317793 manufacture(51048-202)