Label: GUNA-ALLERGY-PREV- ambrosia artemisiifolia - anguilla rostrata blood serum - arundo pliniana root - black currant - chelidonium majus - citric acid monohydrate - histamine dihydrochloride - human interleukin 12 - interferon gamma-1b - manganese gluconate - parietaria officinalis - phleum pratense - sodium pyruvate - sodium sulfate - succinic acid - sulfur - urtica urens - viburnum opulus root - wyethia helenioides root - solution/ drops

  • 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 21, 2018

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  • ACTIVE INGREDIENTS/PURPOSE

    AMBROSIA ARTEMISIIFOLIA 18X RAGWEED SENSITIVITY

    ARUNDO MAURITANICA 18X DETOXIFICATION ACTIVITY

    ASCLEPIAS VINCETOXICUM 6X, 10X, 30X IMMUNE SUPPORT

    BLACK CURRANT 1X DETOXIFICATION ACTIVITY

    CITRICUM ACIDUM 6X ANTIOXIDANT

    HISTAMINUM HYDROCHLORICUM 12X, 30X, 200X ANTIHISTAMINE

    INTERFERON GAMMA 4C IMMUNE SUPPORT

    INTERLEUKIN 12 4C IMMUNE SUPPORT

    MANGANESE GLUCONATE 4X IMMUNE SUPPORT

    NATRUM PYRUVICUM 6X ANTI-ALLERGY

    NATRUM SULF 12X, 30X, 200X METABOLIC SUPPORT

    PARIETARIA OFFICINALIS 18X PELLITORY OF THE WALL SENSITIVITY

    PHLEUM PRATENSE 18X TIMOTHY SENSITIVITY

    SERUM ANGUILLAE 12X, 30X, 200X ANTI-ALLERGY

    SUCCINICUM ACIDUM 6X METABOLIC SUPPORT

    SULFUR 12X, 30X, 200X SKIN DETOXIFICATION

    URTICA URENS 18X NETTLE SENSITIVITY

    VIBURNUM OPULUS T LYMPHATIC SYSTEM DETOXIFICATION

    WYETHIA HELENIOIDES 18X WYETHIA SENSITIVITY




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  • USES

    Temporary relief of allergy symptoms due to exposure to pollen from:

    • Grass
    • Sunflower
    • Nettle



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  • WARNINGS

    • Stop use and ask doctor if symptoms persist more than 5 days.
    • If pregnant or breast-feeding ask a health professional before use.
    • Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
    • Contains ethyl alcohol 30%
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  • PREGNANCY

    If pregnant or breast-feeding ask a doctor before use

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  • WARNINGS

    Keep out of reach of children

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  • DIRECTIONS

    For maximum symptom relief start before the anticipated allergen exposure.


    Adults and children 12 years and older 20 drops in a little water, 2 times per day

    Children between 12 years and 6 years of age 10 drops in a little water, 2 times per day

    Children under 6 years 5 drops in a glass of water, 2 times per day

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  • QUESTIONS

    Questions?: info@gunainc.com, tel. (484) 223-3500

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  • INDICATIONS & USAGE


    Take 15 minutes before meals

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  • INACTIVE INGREDIENT

    Inactive ingredient: Ethyl alcohol 30%.

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  • PRINCIPAL DISPLAY PANEL
  • INGREDIENTS AND APPEARANCE
    GUNA-ALLERGY-PREV 
    ambrosia artemisiifolia - anguilla rostrata blood serum - arundo pliniana root - black currant - chelidonium majus - citric acid monohydrate - histamine dihydrochloride - human interleukin 12 - interferon gamma-1b - manganese gluconate - parietaria officinalis - phleum pratense - sodium pyruvate - sodium sulfate - succinic acid - sulfur - urtica urens - viburnum opulus root - wyethia helenioides root - solution/ drops
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:17089-299
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA - UNII:9W34L2CQ9A) AMBROSIA ARTEMISIIFOLIA 18 [hp_X]  in 30 mL
    ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC) (ARUNDO PLINIANA ROOT - UNII:ZXE7LB03WC) ARUNDO PLINIANA ROOT 18 [hp_X]  in 30 mL
    ASCLEPIAS CURASSAVICA (UNII: JSZ93E47EP) (ASCLEPIAS CURASSAVICA - UNII:JSZ93E47EP) ASCLEPIAS CURASSAVICA 6 [hp_X]  in 30 mL
    BLACK CURRANT (UNII: 9755T40D11) (BLACK CURRANT - UNII:9755T40D11) BLACK CURRANT 1 [hp_X]  in 30 mL
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID 6 [hp_X]  in 30 mL
    HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE 30 [hp_X]  in 30 mL
    INTERFERON GAMMA-1B (UNII: 21K6M2I7AG) (INTERFERON GAMMA-1B - UNII:21K6M2I7AG) INTERFERON GAMMA-1B 4 [hp_C]  in 30 mL
    HUMAN INTERLEUKIN 12 (UNII: 7B590791ER) (HUMAN INTERLEUKIN 12 - UNII:7B590791ER) HUMAN INTERLEUKIN 12 4 [hp_C]  in 30 mL
    MANGANESE GLUCONATE (UNII: 9YY2F980SV) (MANGANESE CATION (2+) - UNII:H6EP7W5457) MANGANESE GLUCONATE 4 [hp_X]  in 30 mL
    SODIUM PYRUVATE (UNII: POD38AIF08) (PYRUVIC ACID - UNII:8558G7RUTR) SODIUM PYRUVATE 6 [hp_X]  in 30 mL
    SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM SULFATE 200 [hp_X]  in 30 mL
    PARIETARIA OFFICINALIS (UNII: 2C839WQ03N) (PARIETARIA OFFICINALIS - UNII:2C839WQ03N) PARIETARIA OFFICINALIS 18 [hp_X]  in 30 mL
    PHLEUM PRATENSE (UNII: S7PW24BX20) (PHLEUM PRATENSE - UNII:S7PW24BX20) PHLEUM PRATENSE 18 [hp_X]  in 30 mL
    ANGUILLA ROSTRATA BLOOD SERUM (UNII: L7B16ESD1U) (ANGUILLA ROSTRATA BLOOD SERUM - UNII:L7B16ESD1U) ANGUILLA ROSTRATA BLOOD SERUM 200 [hp_X]  in 30 mL
    SUCCINIC ACID (UNII: AB6MNQ6J6L) (SUCCINIC ACID - UNII:AB6MNQ6J6L) SUCCINIC ACID 6 [hp_X]  in 30 mL
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 30 [hp_X]  in 30 mL
    URTICA URENS (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9) URTICA URENS 18 [hp_X]  in 30 mL
    VIBURNUM OPULUS ROOT (UNII: T1UG6H6805) (VIBURNUM OPULUS ROOT - UNII:T1UG6H6805) VIBURNUM OPULUS ROOT 3 g  in 30 mL
    WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N) (WYETHIA HELENIOIDES ROOT - UNII:J10PD1AQ0N) WYETHIA HELENIOIDES ROOT 18 [hp_X]  in 30 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:17089-299-18 1 in 1 BOX 12/21/2018
    1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 05/23/2006
    Labeler - Guna spa (430538264)
    Establishment
    Name Address ID/FEI Business Operations
    Guna spa 338587646 manufacture(17089-299)
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