Label: EQUALINE CLINICAL STRENGTH- selenium sulfide liquid 

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

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 02/13

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  • ACTIVE INGREDIENT

    SELENIUM SULFIDE 1%

    PURPOSE

    ANTI-DANDRUFF, ANTI-SEBORRHEIC DERMATITIS

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  • USES

    HELPS PREVENT THE CHANCE OF RECURRENCE OF FLAKING, ITCHING, IRRITATION, SCALING AND REDNESS ASSOCIATED WITH DANDRUFF AND SEBORRHEIC DERMATITIS.

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  • WARNINGS

    FOR EXTERNAL USE ONLY.

    ASK A DOCTOR BEFORE USING IF YOU HAVE

    SEBORRHEIC DERMATITIS IN AREAS OTHER THAN THE SCALP.

    WHEN USING THIS PRODUCT

    AVOID CONTACT WITH EYES. IF PRODUCT GETS INTO EYES, RINSE THOROUGHLY WITH WATER. FOR USE ON COLOR TREATED OR PERMED HAIR, RINSE THOROUGHLY.

    STOP USING THIS PRODUCT 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.

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  • DIRECTIONS

    SHAKE WELL, APPLY SHAMPOO, RINSE THOROUGHLY. FOR BEST RESULTS, USE AT LEAST TWICE A WEEK OR AS DIRECTED BY A DOCTOR.

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  • INACTIVE INGREDIENTS

    WATER (AQUA), AMMONIUM LAURETH SULFATE, AMMONIUM LAURYL SULFATE, GLYCOL DISTEARATE, COCAMIDE MEA, ACRYLATES COPOLYMER, AMMONIUM XYLENESULFONATE, SODIUM CITRATE, FRAGRANCE (PARFUM), DIMETHICONE, CETYL ALCOHOL, SODIUM CHLORIDE, CITRIC ACID, SODIUM BENZOATE, STEARYL ALCOHOL, DISODIUM EDTA, HYDROXYPROPYL METHYLCELLULOSE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, RED 4 (CI 14700).

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  • QUESTIONS OR COMMENTS?

    1-877-932-7948

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  • LABEL COPY
  • INGREDIENTS AND APPEARANCE
    EQUALINE  CLINICAL STRENGTH
    selenium sulfide liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:41163-618
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SELENIUM SULFIDE (SELENIUM SULFIDE) SELENIUM SULFIDE 10 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    AMMONIUM LAURETH-3 SULFATE  
    AMMONIUM LAURYL SULFATE  
    GLYCOL DISTEARATE  
    COCO MONOETHANOLAMIDE  
    METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)  
    AMMONIUM XYLENESULFONATE  
    SODIUM CITRATE  
    DIMETHICONE  
    CETYL ALCOHOL  
    SODIUM CHLORIDE  
    CITRIC ACID MONOHYDRATE  
    SODIUM BENZOATE  
    STEARYL ALCOHOL  
    EDETATE DISODIUM  
    HYPROMELLOSES  
    METHYLCHLOROISOTHIAZOLINONE  
    METHYLISOTHIAZOLINONE  
    FD&C RED NO. 4  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:41163-618-14 420 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part358H 02/14/2013
    Labeler - SUPERVALU INC. (006961411)
    Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
    Establishment
    Name Address ID/FEI Business Operations
    APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture(41163-618)
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