Available Formats

• ACTIVE INGREDIENT

  Active Ingredient                                   Purpose

  Triclosan 0.15%..................................Antibacterial

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• PURPOSE

  Uses

  forthe temporary relief of minor aches and pains of muscles and joints.

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• KEEP OUT OF REACH OF CHILDREN

  Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

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• INDICATIONS & USAGE

  Other information

  • store at 20oC to 25oC (68o to 77oF)

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• WARNINGS

  Warnings

  For external use only. Avoid contact with eyes.

  Ask a doctor before use if you have cough associated with 

  • smoking
  • excessive phlegm
  • asthma
  • emphysema
  • persistent or chronic cough

  When using this product do not

  • heat
  • microwafe
  • add to hot water or any container where healing water may cause splattering and result in burns
  • use in eyes or directly on mucous membranes
  • take by mouth or place in nostrils
  • apply to wounds or damaged skin
  • bandage skin

  Consult a doctor and discontinue use if condition worsesn, persists for more than 1 week or tends to recur.

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• DOSAGE & ADMINISTRATION

  Directions

  • see important warnings under "When using this product"
  • adults & children 2 years of age & older: apply to the affected area not more than 3 to 4 times daily.
  • children under 2 years of age: consult a physician.

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• INACTIVE INGREDIENT

  Inactive Ingredients

  camphor, carbomer, ethyl alcohol, fd&c blue no.1, isopropyl alcohol, methylchloroisothiazolinone, methylisothiazolinone, sodium hydroxide, water.

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• INGREDIENTS AND APPEARANCE

  HAND CLEANSE  REFILL triclosan gel

  Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58503-008 Route of Administration TOPICAL

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 7.5 mg  in 500 mg

  Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)   SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)   SODIUM LAURETH SULFATE (UNII: BPV390UAP0)   COCO DIETHANOLAMIDE (UNII: 92005F972D)   SODIUM CHLORIDE (UNII: 451W47IQ8X)   PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)   CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)   GLYCERIN (UNII: PDC6A3C0OX)   EDETATE DISODIUM (UNII: 7FLD91C86K)   .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)   METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)   FD&C YELLOW NO. 5 (UNII: I753WB2F1M)   METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58503-008-01 500 mg in 1 BOTTLE

  Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 05/24/2013

  Labeler - China Ningbo Shangge Cosmetic Technology Corp. (529287434)

  Establishment
  Name	Address	ID/FEI	Business Operations
  China Ningbo Shangge Cosmetic Technology Corp.		529287434	manufacture(58503-008)

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