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    NDC 61152-0196-18 Snore Stop Extinguisher Throat 6; 6; 6; 12; 6; 6; 6 [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL Details

    Snore Stop Extinguisher Throat 6; 6; 6; 12; 6; 6; 6 [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL

    Snore Stop Extinguisher Throat is a ORAL SPRAY in the HUMAN OTC DRUG category. It is labeled and distributed by Green Pharmaceuticals Inc. The primary component is ATROPA BELLADONNA; EPHEDRA DISTACHYA FLOWERING TWIG; GOLDENSEAL; HISTAMINE DIHYDROCHLORIDE; POTASSIUM DICHROMATE; STRYCHNOS NUX-VOMICA SEED; TEUCRIUM MARUM.

    Product Information

    NDC 61152-0196
    Product ID 61152-196_eadd60e6-8f8c-654e-e053-2a95a90a58eb
    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 Snore Stop Extinguisher Throat
    Proprietary Name Suffix n/a
    Non-Proprietary Name atropa belladonna, ephedra distachya flowering twig, histamine dihydrochloride, goldenseal, potassium dichromate, strychnos nux-vomica seed, teucrium marum
    Product Type HUMAN OTC DRUG
    Dosage Form SPRAY
    Route ORAL
    Active Ingredient Strength 6; 6; 6; 12; 6; 6; 6
    Active Ingredient Units [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL; [hp_X]/4.5mL
    Substance Name ATROPA BELLADONNA; EPHEDRA DISTACHYA FLOWERING TWIG; GOLDENSEAL; HISTAMINE DIHYDROCHLORIDE; POTASSIUM DICHROMATE; STRYCHNOS NUX-VOMICA SEED; TEUCRIUM MARUM
    Labeler Name Green Pharmaceuticals Inc
    Pharmaceutical Class Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 61152-0196-18 (61152019618)

    NDC Package Code 61152-196-18
    Billing NDC 61152019618
    Package 18 mL in 1 BOTTLE, SPRAY (61152-196-18)
    Marketing Start Date 2012-12-28
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 158dc43d-1105-4757-9f3a-dbad961f8bd8 Details

    Revised: 10/2022