Label: CONSTIPATION RELIEF- aluminum oxide, bryonia alba root, sodium chloride, graphite, silicon dioxide pellet

  • NDC Code(s): 61727-304-21
  • 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

If you are a consumer or patient please visit this version.

View All Sections
  • Active Ingredients:

    Alumina 10X, Bryonia alb. 8X, Natrum mur. 8X, Graphites 10X, Silicea 10X.

  • Purpose:

    For the temporary relief of constipation. Non-stimulant, non-habit forming.

  • Keep out of reach of children.

    Keep out of reach of children.

  • 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.

  • Warnings:

    If symptoms persist or worsen, or if pregnant or nursing, consult a doctor.

  • 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.

  • Inactive Ingredients:

    Sucrose/lactose.

  • Constipation Relief

    Constipation Relief

    Homeopathic Medicine

    85 Pellets

    constipation relief image

    hcl_label_constipation-2012.jpg

  • INGREDIENTS AND APPEARANCE
    CONSTIPATION RELIEF 
    aluminum oxide, bryonia alba root, sodium chloride, graphite, silicon dioxide pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61727-304
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM OXIDE (UNII: LMI26O6933) (ALUMINUM OXIDE - UNII:LMI26O6933) ALUMINUM OXIDE10 [hp_X]  in 4 g
    BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT8 [hp_X]  in 4 g
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE8 [hp_X]  in 4 g
    GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE10 [hp_X]  in 4 g
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE10 [hp_X]  in 4 g
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61727-304-214 g in 1 TUBE; Type 0: Not a Combination Product07/05/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/05/2012
    Labeler - Homeocare Laboratories (088248828)
    Registrant - Homeocare Laboratories (088248828)
    Establishment
    NameAddressID/FEIBusiness Operations
    Homeocare Laboratories088248828manufacture(61727-304)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!