Label: EQUATE ANTI DANDRUFF- salicylic acid shampoo

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 29, 2016

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  • Active ingredient

    Salicylic Acid 2%

    Purpose

    Anti-Dandruff/Anti-Seborrheic Dermatitis/Anti-Psoriasis

  • Uses

    controls the symptoms of dandruff, seborrheic dermatitis, and psoriasis.

  • Warnings

    For external use only.

    Ask a doctor before use if you have

    a condition that covers a large area of the body.

    When using this product

    • avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
    • for use on color treated or permed hair, rinse thoroughly.

    Stop use and ask a doctor if

    condition worsens or does not improve after regular use of this product as directed.

    Keep out of reach of children.

    In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

  • Directions

    • for best results, use twice a week or as directed by a doctor.
    • wet hair, massage onto scalp for several minutes, and then rinse.
    • repeat if desired.
  • Inactive ingredients

    Water (Aqua), Sodium Laureth Sulfate, Acrylates Crosspolymer-4, Cocamide MEA, Sodium Cocoyl Sarcosinate, Glycol Distearate, Polyquaternim-7, Fragrance (Parfum), Sodium Chloride, Sodium Hydroxide, Tetrasodium EDTA, BHT, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090).

  • Questions or Comments?

    1-888-287-1915

  • Label Copy

    Image of the label

  • INGREDIENTS AND APPEARANCE
    EQUATE ANTI DANDRUFF 
    salicylic acid shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-450
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
    CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    SODIUM COCOYL SARCOSINATE (UNII: 1R9DUY89CZ)  
    GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
    POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49035-450-07207 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D02/28/2016
    Labeler - WAL-MART STORES INC (051957769)
    Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    APOLLO HEALTH AND BEAUTY CARE201901209manufacture(49035-450)
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