Available Formats

• Drug Facts Box OTC-Active Ingredient Section

  Triclosan 0.3%
  

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• Drug Facts Box OTC-Purpose Section

  Antiseptic

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• Drug Facts Box OTC-Indications & Usage Section

  for hand-washing to decrease bacteria on the skin
  

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• Drug Facts Box OTC-Warnings Section

  For external use only
  

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• Drug Facts Box OTC-When Using Section

  do not get into eyes
  

  if contact occurs, rinse eyes thoroughly with water
  

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• Drug Facts Box OTC-Stop Use Section

  irritation and redness develop
  

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• Drug Facts Box OTC-Keep Out of Reach of Children Section

  if swallowed, get medical help or contact a Poison Control Center right away
  

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• Drug Facts Box OTC-Dosage & Administration Section

  
  wet hands and forearms

  apply 5 milliliters (teaspoonful) or palmful to hands and forearms

  scrub thoroughly for 1 minute and rinse
  

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• Drug Facts Box OTC-Inactive Ingredient Section

  water, sodium laureth sulfate, sodium lauryl sulfate, cocamidopropyl betaine, alcohol denat., propylene glycol, tetrasodium EDTA, PEG-75 lanolin,  boric acid, lauramine oxide, chloroxylenol, methylparaben, propylparaben, fragrance, aloe barbadensis, acid red 1, reactive green 12
  

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• DermaCare 6899 1000ml

  6899M3PE.jpg  DermaCare 1000 ml

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• INGREDIENTS AND APPEARANCE

  DERMACARE  triclosan soap

  Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67147-576 Route of Administration TOPICAL

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.003 mL  in 1 mL

  Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)   PROPYLENE GLYCOL (UNII: 6DC9Q167V3)   SODIUM LAURETH SULFATE (UNII: BPV390UAP0)   COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)   BORIC ACID (UNII: R57ZHV85D4)   ALCOHOL (UNII: 3K9958V90M)   CHLOROXYLENOL (UNII: 0F32U78V2Q)   ALOE VERA LEAF (UNII: ZY81Z83H0X)   PROPYLPARABEN (UNII: Z8IX2SC1OH)   METHYLPARABEN (UNII: A2I8C7HI9T)

  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67147-576-06 1 in 1 BOX 1 800 mL in 1 BAG 2 NDC:67147-576-17 532 mL in 1 BOTTLE, PLASTIC 3 NDC:67147-576-24 118 mL in 1 BOTTLE, PLASTIC 4 NDC:67147-576-01 1200 mL in 1 CARTRIDGE 5 NDC:67147-576-03 350 mL in 1 CARTRIDGE 6 NDC:67147-576-05 540 mL in 1 BOTTLE, PLASTIC 7 NDC:67147-576-07 700 mL in 1 BAG 8 NDC:67147-576-09 2000 mL in 1 CARTRIDGE 9 NDC:67147-576-10 1000 mL in 1 CARTRIDGE 10 NDC:67147-576-11 1000 mL in 1 BOTTLE, PLASTIC 11 NDC:67147-576-12 1000 mL in 1 BAG 12 NDC:67147-576-13 800 mL in 1 BAG 13 NDC:67147-576-14 3785 mL in 1 BOTTLE, PLASTIC 14 NDC:67147-576-15 946 mL in 1 BOTTLE, PLASTIC 15 NDC:67147-576-28 149 mL in 1 BOTTLE, PLASTIC 16 NDC:67147-576-27 800 mL in 1 CARTRIDGE 17 NDC:67147-576-55 208200 mL in 1 DRUM 18 NDC:67147-576-08 1 in 1 BOX 18 1000 mL in 1 BAG 19 NDC:67147-576-16 236 mL in 1 BOTTLE, PLASTIC 20 NDC:67147-576-18 50 mL in 1 BOTTLE, PLASTIC

  Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 07/01/2010

  Labeler - Apple Products, Inc. (965982544)

  Registrant - ABC Compounding Co., Inc. (003284353)

  Establishment
  Name	Address	ID/FEI	Business Operations
  ABC Compounding Co., Inc.		003284353	manufacture

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