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Zep Acclaim (Zep Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 500 mL in 1 BOTTLE, PLASTIC (66949-999-00) Label Information
LIQUID 3785 mL in 1 BOTTLE, PLASTIC (66949-999-21) Label Information
LIQUID 1000 mL in 1 BOTTLE, PLASTIC (66949-999-10) Label Information

Complete Zep Acclaim Information

  • Active ingredient

    Triclosan 0.1%


  • Purpose

    Antiseptic Handwash


  • Uses

    Hand washing to decrease bacteria on skin.


  • Warnings

    For external use only.


  • DO NOT USE

    Do not use in or around eyes.


  • WHEN USING

    When using this product

    • If eye contact occurs, rinse promptly and thoroughly with water.
    • If swallowed, seek medical attention.

  • STOP USE

    Discontinue use if irritation and redness develops. If condition persists for more than 72 hours, consult a doctor.


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.


  • Directions

    • Wet hands with water
    • Place hands under dispenser
    • Apply liquid soap
    • Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles
    • Rinse thoroughly

  • Other information

    • Store at room temperature
    • Do not freeze

  • Inactive ingredients

    Water, Ammonium Lauryl Sulfate, Ammonium Laureth Sulfate, Cocamide DIPA, Ammonium Chloride, Disodium Ricinoleamido MEA Sulfosuccinate,Glycerin, Fragrance, Tetrasodium EDTA, Citric Acid, Methylchloroisothiazolinone (and) Methylisothiazolinone, Glutaral, Yellow 5, Red 4


  • INGREDIENTS AND APPEARANCE
    ZEP ACCLAIM 
    triclosan liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:66949-999
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.01 g  in 10 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    AMMONIUM LAURETH-3 SULFATE (UNII: 896SJ235FN)  
    COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)  
    AMMONIUM CHLORIDE (UNII: 01Q9PC255D)  
    DISODIUM RICINOLEIC MONOETHANOLAMIDE SULFOSUCCINATE (UNII: 1YHW4GJC3U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    GLUTARAL (UNII: T3C89M417N)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66949-999-00 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/29/1995 01/01/2019
    2 NDC:66949-999-10 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/29/1995 01/01/2019
    3 NDC:66949-999-21 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/29/1995 01/01/2019
    4 NDC:66949-999-15 946.353 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/29/1995 01/01/2019
    5 NDC:66949-999-89 1040990 mL in 1 CONTAINER; Type 0: Not a Combination Product 03/29/1995 01/01/2019
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 03/29/1995 01/01/2019
    Labeler - Zep Inc. (030471374)
    Establishment
    Name Address ID/FEI Business Operations
    Zep Inc. 030471374 manufacture(66949-999)