Label: ANTIBACTERIAL FOAMING- triclosan liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 41520-170-08 - Packager: AMERICAN SALES COMPANY
- Category: HUMAN OTC DRUG LABEL
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 January 21, 2011
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- ACTIVE INGREDIENT
- PURPOSE
- USES
- WARNINGS
- DIRECTIONS
- OTHER INFORMATION
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INACTIVE INGREDIENTS
WATER, SODIUM LAURETH SULFATE, GLYCERETH-26, DISODIUM LAURETH SULFOSUCCINATE, COCAMIDOPROPYL BETAINE, FRAGRANCE, PROPYLENE GLYCOL, PANTHENOL, ALOE BARBADENSIS LEAF JUICE, XANTHAN GUM, BENZOPHENONE-4, IMIDAZOLIDYNL UREA, DMDM HYDANTOI N, PEG-120 METHYL GLUCOSE DIOLEATE, PEG-7 GLYCERYL COCOATE, POLYSORBATE 20, TETRASODIUM EDTA, CITRIC ACID, BLUE 1 (CI 42090), YELLOW 10 (CI 47005).
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL FOAMING OLIVE AND ALOE
triclosan liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41520-170 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.3 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) GLYCERETH-26 (UNII: NNE56F2N14) DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PANTHENOL (UNII: WV9CM0O67Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) XANTHAN GUM (UNII: TTV12P4NEE) SULISOBENZONE (UNII: 1W6L629B4K) IMIDUREA (UNII: M629807ATL) DMDM HYDANTOIN (UNII: BYR0546TOW) PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) GLYCERYL COCOATE (UNII: WVK1CT5994) POLYSORBATE 20 (UNII: 7T1F30V5YH) EDETATE SODIUM (UNII: MP1J8420LU) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41520-170-08 236 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 01/21/2011 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