Available Formats

• Active Ingredient

  Tetrahydrozoline HCl 0.5%
  

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• Purpose

  Redness reliever
  

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• Use

  • for the relief of redness of the eye due to minor eye irritations

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• Warnings

  Ask a doctor before use if you have narrow angle glaucoma
  

  When using this product

  • pupils may become enlarged temporarily
  • overuse may cause more eye redness
  • remove contact lenses before using
  • do not use if this solution changes color or become cloudy
  • do not touch tip of container to any surface to avoid contamination
  • replace cap after each use
    

  Stop use and ask a doctor if

  • you feel eye pain
  • changes in vision occur
  • redness or irritation of the eye lasts
  • condition worsens or lasts more than 72 hours
    

  If pregnant or breast-feeding,

  ask a health professional before use.
  

  Keep out of reach of children.

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

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• Directions

  • Put 1 to 2 drops in the affected eye(s) up to 4 times daily
  • children under 6 years of age:  ask a doctor
    

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• Other information

  • store between 15° to 25°C (59°F to 77°F)

    
    

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• Inactive ingredients

  benzalkonium chloride, boric acid, edetate disodium, hydrochloric acid, purified water, sodium borate, sodium chloride
  

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• package label

  Redness relief

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• INGREDIENTS AND APPEARANCE

  REDNESS RELIEVER   tetrahydrozoline hcl liquid

  Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51134-0062 Route of Administration OPHTHALMIC

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE 0.5 mg  in 1 mL

  Inactive Ingredients Ingredient Name Strength BORIC ACID (UNII: R57ZHV85D4)   SODIUM BORATE (UNII: 91MBZ8H3QO)   EDETATE DISODIUM (UNII: 7FLD91C86K)   BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)   SODIUM CHLORIDE (UNII: 451W47IQ8X)   WATER (UNII: 059QF0KO0R)   HYDROCHLORIC ACID (UNII: QTT17582CB)

  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51134-0062-5 1 in 1 BOX 1 15 mL in 1 BOTTLE

  Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part349 08/29/2010

  Labeler - Samchundang Pharm. Co., Ltd. (687792325)

  Registrant - Samchundang Pharm. Co., Ltd. (687792325)

  Establishment
  Name	Address	ID/FEI	Business Operations
  Samchundang Pharm. Co., Ltd.		687792325	manufacture

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