Label: FOAMING HAND WASH- triclosan 0.46% liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 41250-808-96 - Packager: Meijer Distribution
- 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 June 13, 2013
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
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Inactive ingredients
water, sodium laureth sulfate, glcerin, cocamidopropyl betaine, ammonium xylenesulfonate, dipropylene glycol,sodium PCA, polyquaternium-10, fragrance, disodium phosphate, cetyl alcohol, aloe barbadensis leaf juice, citric acid, tetrasodium EDTA, methylchloroisothiazolinone, methylisothiazolinone, green3, yellow 10
- adverse reactions
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
FOAMING HAND WASH
triclosan 0.46% liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-808 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN .46 mg in 1 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) GLYCERIN (UNII: PDC6A3C0OX) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM) DIPROPYLENE GLYCOL (UNII: E107L85C40) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) POLYQUATERNIUM-10 (400 MPA.S AT 2%) (UNII: HB1401PQFS) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) CETYL ALCOHOL (UNII: 936JST6JCN) ALOE VERA LEAF (UNII: ZY81Z83H0X) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE SODIUM (UNII: MP1J8420LU) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-808-96 221.8 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/01/2013 Labeler - Meijer Distribution (006959555) Registrant - Vi-Jon (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon 088520668 manufacture(41250-808)