Label: PMS RELIEF- copper, estrone, histamine dihydrochloride, magnesium phosphate, tribasic, pentahydrate, sodium sulfate pellet

  • NDC Code(s): 61727-310-21
  • 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 26, 2018

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  • Active ingredients:

    Cuprum metallicum 10X, Folliculinum 18X, Histaminum 8X, Mag. phos. 10X, Natrum sulphuricum 8X.

  • Inactive ingredients:

    Sucrose/lactose.

  • Purpose:

    Temporarily relieves bloating, cramping, water retention, breast tenderness, skin blemishes and mood swings associated with menstrual periods.

  • 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.

  • Keep out of reach of children.

    Keep out of reach of children.

  • 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.

  • 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.

  • PMS Relief

    PMS Relief

    Homeopathic Medicine

    85 Pellets

    hcl label pms 2012.jpg

    pms relief image

  • INGREDIENTS AND APPEARANCE
    PMS RELIEF 
    copper, estrone, histamine dihydrochloride, magnesium phosphate, tribasic, pentahydrate, sodium sulfate pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61727-310
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER10 [hp_X]  in 4 g
    ESTRONE (UNII: 2DI9HA706A) (ESTRONE - UNII:2DI9HA706A) ESTRONE18 [hp_X]  in 4 g
    HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE8 [hp_X]  in 4 g
    MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE (UNII: 453COF7817) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE10 [hp_X]  in 4 g
    SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE8 [hp_X]  in 4 g
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61727-310-214 g in 1 TUBE; Type 0: Not a Combination Product07/23/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/23/2012
    Labeler - Homeocare Laboratories (088248828)
    Registrant - Homeocare Laboratories (088248828)
    Establishment
    NameAddressID/FEIBusiness Operations
    Homeocare Laboratories088248828manufacture(61727-310)
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