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    NDC 63479-0103-01 A03 1; 2; 6; 1; 2; 1; 12; 1; 15; 15; 1; 12; 12; 6; 1; 1; 1; 3; 6; 1; 1 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details

    A03 1; 2; 6; 1; 2; 1; 12; 1; 15; 15; 1; 12; 12; 6; 1; 1; 1; 3; 6; 1; 1 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

    A03 is a SUBLINGUAL SOLUTION/ DROPS in the HUMAN OTC DRUG category. It is labeled and distributed by Apex Energetics Inc.. The primary component is ALFALFA; AMERICAN GINSENG; APIS MELLIFERA; ARCTOSTAPHYLOS UVA-URSI LEAF; ASPARAGUS; AVENA SATIVA FLOWERING TOP; BARIUM IODIDE; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA ROOT; CALCIUM HEXAFLUOROSILICATE; CHELIDONIUM MAJUS; CONIUM MACULATUM FLOWERING TOP; F.

    Product Information

    NDC 63479-0103
    Product ID 63479-0103_0e765c65-dfc5-b0fa-e063-6294a90a4b51
    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 A03
    Proprietary Name Suffix ULTRA ANTITOX
    Non-Proprietary Name ALFALFA, AMERICAN GINSENG, APIS MELLIFICA, ASPARAGUS OFFICINALIS, AVENA SATIVA, BARYTA IODATA, BERBERIS VULGARIS, BRYONIA, CARDUUS MARIANUS, CHAMOMILLA, CHELIDONIUM MAJUS, CONIUM MACULATUM, FERRUM IODATUM, LAPIS ALBUS, LYCOPODIUM CLAVATUM, NATRUM CARBONIC
    Product Type HUMAN OTC DRUG
    Dosage Form SOLUTION/ DROPS
    Route SUBLINGUAL
    Active Ingredient Strength 1; 2; 6; 1; 2; 1; 12; 1; 15; 15; 1; 12; 12; 6; 1; 1; 1; 3; 6; 1; 1
    Active Ingredient Units [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
    Substance Name ALFALFA; AMERICAN GINSENG; APIS MELLIFERA; ARCTOSTAPHYLOS UVA-URSI LEAF; ASPARAGUS; AVENA SATIVA FLOWERING TOP; BARIUM IODIDE; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA ROOT; CALCIUM HEXAFLUOROSILICATE; CHELIDONIUM MAJUS; CONIUM MACULATUM FLOWERING TOP; F
    Labeler Name Apex Energetics Inc.
    Pharmaceutical Class Allergens [CS], Allergens [CS], Bee Venoms [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 Alle
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2025-12-31

    Package

    NDC 63479-0103-01 (63479010301)

    NDC Package Code 63479-0103-1
    Billing NDC 63479010301
    Package 30 mL in 1 BOTTLE, GLASS (63479-0103-1)
    Marketing Start Date 1994-12-15
    NDC Exclude Flag N
    Pricing Information N/A
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