Label: MARKET BASKET ULTRA- triclosan soap
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Contains inactivated NDC Code(s)
NDC Code(s): 63691-023-12 - Packager: Sun Products Corporation
- 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 December 30, 2014
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- Official Label (Printer Friendly)
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ACTIVE INGREDIENT
Active ingredient
Triclosan 0.10%
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. In case of eye contact, rinse thoroughly with water.
Inactive ingredients Water, Sodium Dodecylbenzenesulfonate, Sodium Laureth Sulfate, Sodium Methyl 2-Sulfopalmitate, Magnesium Sulfate, Sodium Xylenesulfonate, Alcohol Denat., Fragrance, Disodium 2-Sulfopalmitate, Methyl Palmitate, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Benzophenone-4, D&C Orange No. 4, Sodium Citrate
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INGREDIENTS AND APPEARANCE
MARKET BASKET ULTRA
triclosan soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63691-023 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.1 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) MAGNESIUM SULFATE (UNII: DE08037SAB) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) ALCOHOL (UNII: 3K9958V90M) DISODIUM 2-SULFOPALMITATE (UNII: VS9295575T) METHYL PALMITATE (UNII: DPY8VCM98I) EDETATE SODIUM (UNII: MP1J8420LU) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) SULISOBENZONE (UNII: 1W6L629B4K) D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U) SODIUM CITRATE (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63691-023-12 591 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 07/01/2014 Labeler - Sun Products Corporation (070931480) Registrant - Demoulas Supermarkets (007869647) Establishment Name Address ID/FEI Business Operations Sun Products Corporation - Salt Lake City 096752865 manufacture(63691-023) Establishment Name Address ID/FEI Business Operations Sun Products Corporation - Bowling Green 809709314 manufacture(63691-023)