Label: HAIR-X HAIR LOSS RELIEF- cadmium sulfate, graphite, phosphoric acid, silicon dioxide, selenium, thallium, ustilago maydis pellet

  • NDC Code(s): 61727-319-21
  • Packager: Homeocare Laboratories
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated December 31, 2018

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  • Active Ingredients:

    Cadmium sulph. 12C, Graphites 4C, Phosphoricum acidum 5C, Silicea 4C, Selenium 5C, Thallium met. 7C, Ustilago 9C.

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  • Inactive Ingredients:

    Sucrose/lactose.

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  • Keep out of reach of children.

    Keep out of reach of children.

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  • Purpose:

    Hair loss-Alopecia.

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  • Indications & Usage:

    Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

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  • Dosage & Administration:

    Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

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  • Warnings:

    If symptoms persist or worsen, or if pregnant or nursing, consult a doctor. Keep out of reach of children. Do not use if cap seal is broken or missing.

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  • Hair-X Hair Loss Relief

    Hair-X Hair Loss Relief

    Homeopathic Medicine

    85 Pellets
    hair-x hair loss relief
    hcl_label_hairx 2012.jpg

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  • INGREDIENTS AND APPEARANCE
    HAIR-X HAIR LOSS RELIEF 
    cadmium sulfate, graphite, phosphoric acid, silicon dioxide, selenium, thallium, ustilago maydis pellet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:61727-319
    Route of Administration SUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CADMIUM SULFATE (UNII: 947UNF3Z6O) (CADMIUM CATION - UNII:T494FZ4G8G) CADMIUM SULFATE 12 [hp_C]  in 4 g
    GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE 4 [hp_C]  in 4 g
    PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 5 [hp_C]  in 4 g
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 4 [hp_C]  in 4 g
    SELENIUM (UNII: H6241UJ22B) (SELENIUM - UNII:H6241UJ22B) SELENIUM 5 [hp_C]  in 4 g
    THALLIUM (UNII: AD84R52XLF) (THALLIUM - UNII:AD84R52XLF) THALLIUM 7 [hp_C]  in 4 g
    USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS 9 [hp_C]  in 4 g
    Inactive Ingredients
    Ingredient Name Strength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE (UNII: J2B2A4N98G)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:61727-319-21 4 g in 1 TUBE; Type 0: Not a Combination Product 07/10/2012
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 07/10/2012
    Labeler - Homeocare Laboratories (088248828)
    Registrant - Homeocare Laboratories (088248828)
    Establishment
    Name Address ID/FEI Business Operations
    Homeocare Laboratories 088248828 manufacture(61727-319)
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