Label: ANTIBACTERIAL MANDARIN AND POMELO- triclosan liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 41520-293-08 - 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 April 1, 2011
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- ACTIVE INGREDIENT
- PURPOSE
- USES
- WARNINGS
- DIRECTIONS
- OTHER INFORMATION
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INACTIVE INGREDIENTS
WATER, SODIUM LAURETH SULFATE, COCAMIDOPROPYL BETAINE, DECYL GLUCOSIDE, PEG-120 METHYL GLUCOSE DIOLEATE, POLYQUATERNIUM-7, CITRUS GRANDIS (POMELO) EXTRACT, CITRUS NOBILIS (MANDARIN) FRUIT EXTRACT, PEG-7 GLYCERYL COCOATE, FRAGRANCE (PARFUM), PEG-40 HYDROGENATED CASTOR OIL, TETRASODIUM EDTA, DMDM HYDANTOIN, CITRIC ACID, SODIUM CHLORIDE, YELLOW 5 (CI 19140), RED 4 (CI 14700), RED 33 (CI 17200).
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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL MANDARIN AND POMELO
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41520-293 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.15 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y) PUMMELO (UNII: ET1TN5W71X) CITRUS NOBILIS (UNII: 8MFF77J91V) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) EDETATE SODIUM (UNII: MP1J8420LU) DMDM HYDANTOIN (UNII: BYR0546TOW) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) SODIUM CHLORIDE (UNII: 451W47IQ8X) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C RED NO. 4 (UNII: X3W0AM1JLX) D&C RED NO. 33 (UNII: 9DBA0SBB0L) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41520-293-08 236 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 04/01/2011 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