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    NDC 66492-0006-02 ALLERGY DROPS 2; 12; 6; 3; 4; 6; 3; 6; 3 [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

    ALLERGY DROPS 2; 12; 6; 3; 4; 6; 3; 6; 3 [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

    ALLERGY DROPS is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Be Well Medical dba Richard Clement Nutrition y Be Well Homeopathics. The primary component is APIS MELLIFERA; APIS MELLIFERA VENOM; EUPHORBIA RESINIFERA RESIN; EUPHRASIA STRICTA; HEDERA HELIX FLOWERING TWIG; HISTAMINE DIHYDROCHLORIDE; ONION; PULSATILLA VULGARIS; SCHOENOCAULON OFFICINALE SEED.

    Product Information

    NDC 66492-0006
    Product ID 66492-006_d449d3d9-49c8-2a4b-e053-2995a90a5a95
    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 DROPS
    Proprietary Name Suffix n/a
    Non-Proprietary Name Apis mellifica, Apisinum, Allium cepa, Euphrasia, Sabadilla, Euphorbium, Pulsatilla, Hedera helix, Histaminum.
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 2; 12; 6; 3; 4; 6; 3; 6; 3
    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
    Substance Name APIS MELLIFERA; APIS MELLIFERA VENOM; EUPHORBIA RESINIFERA RESIN; EUPHRASIA STRICTA; HEDERA HELIX FLOWERING TWIG; HISTAMINE DIHYDROCHLORIDE; ONION; PULSATILLA VULGARIS; SCHOENOCAULON OFFICINALE SEED
    Labeler Name Be Well Medical dba Richard Clement Nutrition y Be Well Homeopathics
    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 2024-12-31

    Package

    NDC 66492-0006-02 (66492000602)

    NDC Package Code 66492-006-02
    Billing NDC 66492000602
    Package 58.5 mL in 1 BOTTLE, DROPPER (66492-006-02)
    Marketing Start Date 2000-01-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 285996bb-e33d-4982-8282-05283f4e4c79 Details

    Revised: 12/2021