Label: ANTIBACTERIAL FOAMING CRANBERRY- triclosan liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 41250-186-08 - Packager: MEIJER DISTRIBUTION 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 November 16, 2011
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- ACTIVE INGREDIENT
- PURPOSE
- USES
- WARNINGS
- DIRECTIONS
- OTHER INFORMATION
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INACTIVE INGREDIENTS
WATER (AQUA), SODIUM XYLENE SULFONATE, DIPROPYLENE GLYCOL, GLYCERIN, SODIUM PCA, AMMONIUM LAURYL SULFATE, COCAMIDOPROPYL BETAINE, POLYQUATERNIUM-10, FRAGRANCE (PARFUM), VACCINIUM MACROCARPON (CRANBERRY) FRUIT EXTRACT, TOCOPHERYL ACETATE, CAMELLIA OLEIFERA (TEA) LEAF EXTRACT, ALOE BARBADENSIS (ALOE VERA) LEAF EXTRACT, DISODIUM PHOSPHATE, CETYL ALCOHOL, PROPYLENE GLYCOL, CITRIC ACID, METHYLPARABEN, PROPYLPARABEN, RED 33 (CI 17200), ORANGE 4 (15510).
- Label copy
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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL FOAMING CRANBERRY
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-186 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.46 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) DIPROPYLENE GLYCOL (UNII: E107L85C40) GLYCERIN (UNII: PDC6A3C0OX) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS) CRANBERRY (UNII: 0MVO31Q3QS) TOCOPHEROL (UNII: R0ZB2556P8) CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60) ALOE VERA LEAF (UNII: ZY81Z83H0X) SODIUM PHOSPHATE (UNII: SE337SVY37) C12-16 ALCOHOLS (UNII: S4827SZE3L) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) D&C RED NO. 33 (UNII: 9DBA0SBB0L) D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-186-08 221 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 11/18/2011 Labeler - MEIJER DISTRIBUTION INC (006959555) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture