DANDRUFF RELIEF DAYLOGIC (SALICYLIC ACID 3.0%) LIQUID [RITE AID]

DANDRUFF RELIEF DAYLOGIC (SALICYLIC ACID 3.0%) LIQUID [RITE AID]
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NDC 11822-1237-3
Set ID 8d173e79-6459-4545-84fe-d9817a309b69
Category HUMAN OTC DRUG LABEL
Packager Rite Aid
Generic Name
Product Class
Product Number
Application Number PART358H
  • ACTIVE INGREDIENT

    Active ingredient                                    Purpose
    Salicylic Acid 3%.................................... Psoriasis, Anti-dandruff,
                                                                  and Seborrheic dermatitis

  • PURPOSE

  • INDICATIONS & USAGE

    Uses
    Relieves and controls the following symptoms associated with
    dandruff, seborrheic dermatitis and psoriasis
    • scalp itching • flaking • irritation • redness • scaling

  • WARNINGS

    Warnings
    For external use only
    Flammable - store away from fire or flame.
    Allergy alert: do not use if allergic to salicylates or aspirin.
    Consult a doctor before use
    • if condition covers a large area of the body.
    Stop use and consult a doctor
    • if condition worsens or does not improve with regular use of
    this product as directed.
    When using this product
    • avoid contact with eyes. If contact occurs, rinse eyes
    thoroughly with water.
    Keep out of the reach of children. If swallowed get medical
    help or contact a Poison Control Center right away. If pregnant
    or breast-feeding consult a health care professional before use.

  • KEEP OUT OF REACH OF CHILDREN

  • DOSAGE & ADMINISTRATION

    Directions
    • Apply to affected areas 1 to 4 times daily or as directed by a doctor.

  • INACTIVE INGREDIENT

    Inactive ingredients
    Aloe Barbadensis Leaf Extract, Melaleuca Alternifolia (Tea Tree)
    Leaf Oil, Menthol, Propylene Glycol, SD Alcohol 40-B,
    Tocopheryl Acetate, Water.

  • PRINCIPAL DISPLAY PANEL

    image descriptionimage description

  • INGREDIENTS AND APPEARANCE
    DANDRUFF RELIEF  DAYLOGIC
    salicylic acid 3.0% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-1237
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) Salicylic Acid3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    Menthol (UNII: L7T10EIP3A)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    ALCOHOL (UNII: 3K9958V90M)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-1237-374 mL in 1 BOTTLE; Type 0: Not a Combination Product09/30/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart358H09/30/2016
    Labeler - Rite Aid (014578892)
    Registrant - Product Quest Mfg (927768135)
    Establishment
    NameAddressID/FEIBusiness Operations
    Product Quest Mfg927768135manufacture(11822-1237) , label(11822-1237)

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