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    NDC 43742-2088-01 Gum Therapy 12; 3; 12; 8; 12; 1; 3; 6; 12; 6; 12; 6; 3; 6 [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

    Gum Therapy 12; 3; 12; 8; 12; 1; 3; 6; 12; 6; 12; 6; 3; 6 [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

    Gum Therapy is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Deseret Biologicals. The primary component is ACONITUM NAPELLUS WHOLE; ARNICA MONTANA WHOLE; BISMUTH SUBNITRATE; CALCIUM FLUORIDE; CALCIUM SULFIDE; CALENDULA OFFICINALIS FLOWERING TOP; DIBASIC POTASSIUM PHOSPHATE; HELIANTHEMUM CANADENSE; MERCURY; MYRRH; SEPIA OFFICINALIS JUICE; SODIUM BORATE; SODIUM .

    Product Information

    NDC 43742-2088
    Product ID 43742-2088_743a5183-1c70-4a47-9945-f6f41eea0531
    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 Gum Therapy
    Proprietary Name Suffix n/a
    Non-Proprietary Name Calendula Officinalis, Kali Phosphoricum, Natrum Muriaticum, Arnica Montana, Borax, Cistus Canadensis, Kreosotum, Myrrha, Calcarea Fluorica, Aconitum Napellus, Bismuthum Subnitricum, Sepia, Hepar Sulphuris Calcareum, Mercurius Vivus
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 12; 3; 12; 8; 12; 1; 3; 6; 12; 6; 12; 6; 3; 6
    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
    Substance Name ACONITUM NAPELLUS WHOLE; ARNICA MONTANA WHOLE; BISMUTH SUBNITRATE; CALCIUM FLUORIDE; CALCIUM SULFIDE; CALENDULA OFFICINALIS FLOWERING TOP; DIBASIC POTASSIUM PHOSPHATE; HELIANTHEMUM CANADENSE; MERCURY; MYRRH; SEPIA OFFICINALIS JUICE; SODIUM BORATE; SODIUM
    Labeler Name Deseret Biologicals
    Pharmaceutical Class Bismuth [CS], Bismuth [EPC]
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 43742-2088-01 (43742208801)

    NDC Package Code 43742-2088-1
    Billing NDC 43742208801
    Package 30 mL in 1 BOTTLE, DROPPER (43742-2088-1)
    Marketing Start Date 2023-07-19
    NDC Exclude Flag N
    Pricing Information N/A
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