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    NDC 69676-0071-01 Allergy D 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 Details

    Allergy D 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1

    Allergy D is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by Genexa Inc.. The primary component is AMBROSIA ARTEMISIIFOLIA; ARUNDO PLINIANA ROOT; BLACK MUSTARD SEED; EUPHRASIA STRICTA; LOBARIA PULMONARIA; ONION; PULSATILLA PRATENSIS; RANUNCULUS BULBOSUS; SCHOENOCAULON OFFICINALE SEED; SOLANUM DULCAMARA STEM; STRYCHNOS NUX-VOMICA SEED; WYETHIA HELENIOID.

    Product Information

    NDC 69676-0071
    Product ID 69676-0071_b5fe1de9-4fef-f9cb-e053-2995a90a0213
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Allergy D
    Proprietary Name Suffix n/a
    Non-Proprietary Name Allium cepa, Ambrosia artemisiifolia, Arundo mauritanica, Dulcamara, Euphrasia officinalis, Nux vomica, Pulsatilla, Ranunculus bulbosus, Sabadilla, Sinapis nigra, Sticta pulmonaria, Wyethia helenoides
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, CHEWABLE
    Route ORAL
    Active Ingredient Strength 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12
    Active Ingredient Units [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
    Substance Name AMBROSIA ARTEMISIIFOLIA; ARUNDO PLINIANA ROOT; BLACK MUSTARD SEED; EUPHRASIA STRICTA; LOBARIA PULMONARIA; ONION; PULSATILLA PRATENSIS; RANUNCULUS BULBOSUS; SCHOENOCAULON OFFICINALE SEED; SOLANUM DULCAMARA STEM; STRYCHNOS NUX-VOMICA SEED; WYETHIA HELENIOID
    Labeler Name Genexa Inc.
    Pharmaceutical Class Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [E
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through n/a

    Package

    NDC 69676-0071-01 (69676007101)

    NDC Package Code 69676-0071-1
    Billing NDC 69676007101
    Package 1 BOTTLE, PLASTIC in 1 CARTON (69676-0071-1) / 60 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC
    Marketing Start Date 2016-03-21
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 2eb9d41b-fd68-738e-e054-00144ff88e88 Details

    Revised: 12/2020