Label: CARE ONE ANTIBACTERIAL TANGERINE SPICE- triclosan liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 41520-191-08 - Packager: AMERICAN SALES COMPANY
- 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 September 27, 2012
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- ACTIVE INGREDIENT
- USES
- WARNINGS
- DIRECTIONS
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INACTIVE INGREDIENT
WATER, SODIUM XYLENESULFONATE, GLYCERIN, DIPROPYLENE GLYCOL, COCAMIDOPROPYL BETAINE, SODIUM LAURETH SULFATE, DISODIUM PHOSPHATE, FRAGRANCE (PARFUM), METHYLPARABEN, PROPYLPARABEN, POLYSORBATE-20, SODIUM PCA, POLYQUATERNIUM-10, TOCOPHERYL ACETATE, CITRIC ACID, CETYL ALCOHOL, RED 33 (CI 17200), ORANGE 4 (CI 15510).
- LABEL COPY
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INGREDIENTS AND APPEARANCE
CARE ONE ANTIBACTERIAL TANGERINE SPICE
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41520-191 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 3 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER BUFFALO (UNII: 0A4PW6CRAI) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) GLYCERIN (UNII: PDC6A3C0OX) DIPROPYLENE GLYCOL (UNII: E107L85C40) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) POLYSORBATE 20 (UNII: 7T1F30V5YH) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CETYL ALCOHOL (UNII: 936JST6JCN) 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:41520-191-08 237 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 09/27/2012 Labeler - AMERICAN SALES COMPANY (809183973) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture(41520-191)