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THERA Antimicrobial Body Cleanser (McKesson Medical-Surgical Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 118 mL in 1 BOTTLE, PLASTIC (68599-0201-4) Label Information
LIQUID 237 mL in 1 BOTTLE, PLASTIC (68599-0201-6) Label Information

Complete THERA Antimicrobial Body Cleanser Information

  • Active ingredient

    Benzalkonium Chloride  0.13%


  • Purpose

    Antiseptic


  • Keep out of reach of children.

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


  • Uses

    • a no-rinse topical antiseptic that reduces and inhibits bacterial growth.

  • Warnings

    For external use only

    Do not use on
    • deep or puncture wounds
    • animal bites
    • serious burns

  • When using this product

    • do not get into eyes

    Stop use and ask a doctor if
    • condition worsens
    • symptoms last more than 7 days or clear up and occur again within a few days

  • Directions

    • Spray soiled and/or odorous (body and/or perineal) areas
    • Gently wipe clean
    • Repeat as necessary until all soils are removed and skin is clean
    • Pat dry. No rinsing necessary.
    • Apply a protectant cream or paste as necessary

  • Other information

    • Protect from freezing. Avoid excessive heat.

  • Inactive ingredients

    Aloe Barbadensis (Aloe Vera) Leaf Juice, SAFFLEXTM (Consisting of Calcium Pantothenate (Vitamin B5), Maltodextrin, Niacinamide (Vitamin B3), Pyridoxine HCl (Vitamin B6), Silica, Sodium Ascorbyl Phosphate, (Vitamin C), Sodium Starch Octenylsuccinate, Tocopheryl Acetate (VItamin E)), Bisabolol, Butylene Glycol, Carthamus Tinctorius (Safflower) Oleosomes, Disodium EDTA, Glycerin, Lavender Ylang Fragrance, Phenoxyethanol, Polysorbate 20, Purified Water, Sodium Hyaluronate, Sodium Hydroxide, Zingiber Officinale (Ginger) Root Extract.


  • Label (4 fl oz)

    image of 4 fl oz label


  • Label (8 fl oz)

    image of 8 fl oz label


  • INGREDIENTS AND APPEARANCE
    THERA ANTIMICROBIAL BODY CLEANSER 
    benzalkonium chloride liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:68599-0201
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 uL  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CALCIUM PANTOTHENATE (UNII: 568ET80C3D)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)  
    SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    WATER (UNII: 059QF0KO0R)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    GINGER (UNII: C5529G5JPQ)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68599-0201-4 118 mL in 1 BOTTLE, PLASTIC
    2 NDC:68599-0201-6 237 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 09/01/2011
    Labeler - McKesson Medical-Surgical Inc. (023904428)
    Registrant - PureTek Corporation (785961046)
    Establishment
    Name Address ID/FEI Business Operations
    PureTek Corporation 785961046 manufacture, label, pack, outsourcing human drug compounding, relabel, repack