Label: DANDRUFF RELIEF DAYLOGIC- salicylic acid 3.0% liquid

  • 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 June 21, 2018

If you are a consumer or patient please visit this version.

View All Sections
  • 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)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!