Label: ELBERRY UP- sambucus nigra, sulphur, bryonia tablet

  • NDC Code(s): 34666-311-01
  • Packager: Nartex Laboratorios Homeopaticos SA DE CV
  • 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 12, 2024

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

  • Drug Facts

  • Active Ingredients

    Sambucus Nigra 6x HPUS*

    Bryonia 6x HPUS*

    Sulphur 12x HPUS*

    The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States. "X" is a homeopathic dilution. See www.nartexlabsusa.com for more information.

  • Purpose

    Sambucus Nigra 6x HPUS*..............Nasal Congestion

    Bryonia 6x HPUS*..............Nasal Congestion and antitussive

    Sulphur 12x HPUS*..............Nasal Congestion and anti-inflammatory

  • Uses

    Temporarily relieves discomforting symptoms such as:

    • runny nose
    • sore throat
    • coughing
    • sneezing and nasal congestion

    Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by FDA, and product has not been clinically tested.

  • Warnings

  • DO NOT USE

    Do not useif you have if you have an allergy or hypersensitivity to the components of the formula or have had a prior reaction to this product.

  • STOP USE

    Stop use and ask a doctor if

    - condition worsens

    - symptoms persist for more than 7 days or clear up and occur again within a few days.

    - rash develops

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding, consult a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    - adults and children 4 years of age and older: take 2 tablets every 6 hours.

    - children under 4 years of age, consult a physician.

  • Other Information

    - store in a cool dry place.

    - do not use if blister pack is broken.

  • Inactive Ingredients

    Gelatin, lactose, magnesium stearate, potato starch, purified water, sodum benzoate, talc

  • Questions or Comments?

    informacion@nartexlabs.com or call 1-877-248-1970 between 9am and 5pm CST. Active ingredients are prepared in accordance with the Homeopathic Pharmacopoeia of the United States, and are therefore non-toxic and have no known side effects. Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by FDA , and product has not been clinically tested.

  • PRINCIPAL DISPLAY PANEL

    PDP

  • INGREDIENTS AND APPEARANCE
    ELBERRY UP 
    sambucus nigra, sulphur, bryonia tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:34666-311
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U) (SAMBUCUS NIGRA FLOWERING TOP - UNII:CT03BSA18U) SAMBUCUS NIGRA FLOWERING TOP6 [hp_X]
    BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT6 [hp_X]
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR12 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    TALC (UNII: 7SEV7J4R1U)  
    GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    STARCH, POTATO (UNII: 8I089SAH3T)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Colorwhite (NONE) Scoreno score
    ShapeROUND (NONE) Size10mm
    FlavorImprint Code none
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:34666-311-011 in 1 CARTON09/03/202011/19/2024
    160 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/03/202011/19/2024
    Labeler - Nartex Laboratorios Homeopaticos SA DE CV (589914576)
    Registrant - Nartex Laboratorios Homeopaticos SA DE CV (589914576)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nartex Laboratorios Homeopaticos SA DE CV589914576manufacture(34666-311)