Label: FEIX FACIAL- sulfur liquid

  • NDC Code(s): 66854-024-01
  • Packager: SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS
  • 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 7, 2012

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  • ACTIVE INGREDIENT

    Feix Facial Liquid soap contains TRICLOSAN, a powerful antibacterial agent. Another one of its components is the active DIPYRITHIONE and BIO-SULFUR used to eliminate Gram positive and Gram negative germs and has a selective action against certain types of fungi.

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  • PURPOSE

    Washing of the face during the dermal infectiuos process of the skin; washing of the skin as a complement for the medical prescription. Please visit your doctor when the dermal process requires a medical diagnosis


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  • KEEP OUT OF REACH OF CHILDREN

    Keep this product out of the reach of children


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  • INDICATIONS & USAGE

    Facial soap used in persons with oily skin.

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  • WARNINGS

    Please suspend its use if you notice an unfavorable reaction on the skin
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  • DOSAGE & ADMINISTRATION

    Apply an adequate amount on wet skin; create foam rubbing the skin very gently; rinse thoroughly, dry patting softly and seal with Calendula Cream for oily skin.

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  • INACTIVE INGREDIENT

    Contains calendula extract, nettle extract, chamomile extract, and following propierties to improve the condition of the skin: anti-inflamatory, aids in cicatrization, astringent, anti-seborrheic, soothing and also tones the skin.

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  • PRINCIPAL DISPLAY PANEL

    IMAGE OF THE LABEL

    IMAGE OF THE LABEL


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  • INGREDIENTS AND APPEARANCE
    FEIX  FACIAL
    sulfur liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:66854-024
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 0.2 mL  in 100 mL
    DIPYRITHIONE (UNII: 9L87N86R9A) (DIPYRITHIONE - UNII:9L87N86R9A) DIPYRITHIONE 0.5 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    COCO DIETHANOLAMIDE (UNII: 92005F972D)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X)  
    CHINESE CINNAMON (UNII: WS4CQ062KM)  
    GINGER (UNII: C5529G5JPQ)  
    GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    GLYCERYL OLEATE (UNII: 4PC054V79P)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    CHAMOMILE (UNII: FGL3685T2X)  
    URTICA DIOICA LEAF (UNII: X6M0DRN46Q)  
    TRICLOSAN (UNII: 4NM5039Y5X)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66854-024-01 280 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part358H 06/30/2012
    Labeler - SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS (880172184)
    Registrant - SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS (880172184)
    Establishment
    Name Address ID/FEI Business Operations
    SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS 880172184 analysis, label, manufacture, pack
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