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    NDC 68770-0190-42 Macula 12; 10; 11; 7; 9 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 Details

    Macula 12; 10; 11; 7; 9 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1

    Macula is a ORAL PELLET in the HUMAN OTC DRUG category. It is labeled and distributed by Natural Ophthalmics, Inc. The primary component is CALCIUM FLUORIDE; CALCIUM PHOSPHATE; CARBON DISULFIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE.

    Product Information

    NDC 68770-0190
    Product ID 68770-190_0dd7c659-d4e2-4616-e063-6394a90a059d
    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 Macula
    Proprietary Name Suffix n/a
    Non-Proprietary Name calcium fluoride, calcium phosphate, carbon disulfide, dibasic potassium phosphate, sodium chloride
    Product Type HUMAN OTC DRUG
    Dosage Form PELLET
    Route ORAL
    Active Ingredient Strength 12; 10; 11; 7; 9
    Active Ingredient Units [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
    Substance Name CALCIUM FLUORIDE; CALCIUM PHOSPHATE; CARBON DISULFIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE
    Labeler Name Natural Ophthalmics, Inc
    Pharmaceutical Class Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 68770-0190-42 (68770019042)

    NDC Package Code 68770-190-42
    Billing NDC 68770019042
    Package 600 PELLET in 1 BOTTLE (68770-190-42)
    Marketing Start Date 2022-04-27
    NDC Exclude Flag N
    Pricing Information N/A
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