Search by Drug Name or NDC

    NDC 59883-0030-04 FLUORIDEX 50; 5 mg/g; mg/g Details

    FLUORIDEX 50; 5 mg/g; mg/g

    FLUORIDEX is a DENTAL PASTE, DENTIFRICE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by DENT-MAT HOLDINGS, LLC.. The primary component is POTASSIUM NITRATE; SODIUM FLUORIDE.

    Product Information

    NDC 59883-0030
    Product ID 59883-030_020d58ac-51bc-19a2-e063-6394a90aedf6
    Associated GPIs 88409902774420
    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 FLUORIDEX
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sodium Fluoride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form PASTE, DENTIFRICE
    Route DENTAL
    Active Ingredient Strength 50; 5
    Active Ingredient Units mg/g; mg/g
    Substance Name POTASSIUM NITRATE; SODIUM FLUORIDE
    Labeler Name DENT-MAT HOLDINGS, LLC.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category UNAPPROVED DRUG OTHER
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 59883-0030-04 (59883003004)

    NDC Package Code 59883-030-04
    Billing NDC 59883003004
    Package 1 TUBE in 1 BOX (59883-030-04) / 112 g in 1 TUBE
    Marketing Start Date 2017-01-06
    NDC Exclude Flag N
    Pricing Information N/A
    << 59883-0020-04 59883-0031-04 >>

    Contents