Label: KROGER MEDICATED DANDRUFF- selenium sulfide 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 25, 2014

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  • ACTIVE INGREDIENT
    SELENIUM SULFIDE 1% PURPOSE - ANTI-DANDRUFF/ANTI-SEBORRHEIC DERMATITIS
  • USES
    FOR THE RELIEF OF FLAKING AND ITCHING ASSOCIATED WITH DANDRUFF AND SEBORRHEIC DERMATITIS AND TO HELP PREVENT THE CHANCE OF RECURRENCE
  • WARNINGS
    FOR EXTERNAL USE ONLY - ASK A DOCTOR BEFORE USE IF YOU HAVE - SEBORRHEIC DERMATITIS IN AREAS OTHER THAN THE SCALP - WHEN USING THIS PRODUCT - AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES ...
  • DIRECTIONS
    SHAKE WELL, APPLY SHAMPOO AND RINSE THOROUGHLY. FOR BEST RESULTS, USE AT LEAST TWICE A WEEK OR AS DIRECTED BY A DOCTOR
  • OTHER INFORMATION
    STORE AT ROOM TEMPERATURE
  • INACTIVE INGREDIENTS
    WATER (AQUA), SODIUM LAURETH SULFATE, TEA-LAURYL SULFATE, COCAMIDOPROPYL BETAINE, ACRYLATES COPOLYMER, CITRIC ACID, FRAGRANCE, AMMONIUM CHLORIDE, DMDM HYDANTOIN, MENTHOL, SODIUM HYDROXIDE ...
  • QUESTIONS OR COMMENTS?
    1-800-632-6900
  • LABEL COPY
    IMAGE OF THE LABEL
  • INGREDIENTS AND APPEARANCE
    Product Information
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