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    NDC 17312-0178-99 Dryness Relief 12; 8; 10; 6; 9; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details

    Dryness Relief 12; 8; 10; 6; 9; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

    Dryness Relief is a OPHTHALMIC LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by TRP Company. The primary component is NUTMEG; RUTA GRAVEOLENS FLOWERING TOP; SILVER; SODIUM CHLORIDE; SULFUR; ZINC.

    Product Information

    NDC 17312-0178
    Product ID 17312-178_f44e0c07-056e-b0f5-e053-2a95a90a96ef
    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 Dryness Relief
    Proprietary Name Suffix n/a
    Non-Proprietary Name SILVER, SODIUM CHLORIDE, NUTMEG, RUTA GRAVEOLENS, SULFUR, ZINC
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route OPHTHALMIC
    Active Ingredient Strength 12; 8; 10; 6; 9; 12
    Active Ingredient Units [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
    Substance Name NUTMEG; RUTA GRAVEOLENS FLOWERING TOP; SILVER; SODIUM CHLORIDE; SULFUR; ZINC
    Labeler Name TRP Company
    Pharmaceutical Class Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Non-Standardized Food Allerg
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 17312-0178-99 (17312017899)

    NDC Package Code 17312-178-99
    Billing NDC 17312017899
    Package 1 BOTTLE, DROPPER in 1 PACKAGE (17312-178-99) / 2.5 mL in 1 BOTTLE, DROPPER
    Marketing Start Date 2023-02-09
    NDC Exclude Flag N
    Pricing Information N/A
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