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    NDC 81740-0002-01 Auraglow Daily 2.43 mg/g Details

    Auraglow Daily 2.43 mg/g

    Auraglow Daily is a DENTAL PASTE, DENTIFRICE in the HUMAN OTC DRUG category. It is labeled and distributed by Auraglow LLC. The primary component is SODIUM FLUORIDE.

    Product Information

    NDC 81740-0002
    Product ID 81740-002_1a8ffb75-e8f5-4b32-9eee-2f47d0b61182
    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 Auraglow Daily
    Proprietary Name Suffix n/a
    Non-Proprietary Name SODIUM FLUORIDE
    Product Type HUMAN OTC DRUG
    Dosage Form PASTE, DENTIFRICE
    Route DENTAL
    Active Ingredient Strength 2.43
    Active Ingredient Units mg/g
    Substance Name SODIUM FLUORIDE
    Labeler Name Auraglow LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part355
    Listing Certified Through 2023-12-31

    Package

    NDC 81740-0002-01 (81740000201)

    NDC Package Code 81740-002-01
    Billing NDC 81740000201
    Package 1 TUBE in 1 CARTON (81740-002-01) / 113 g in 1 TUBE
    Marketing Start Date 2021-08-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL f9924be1-5467-4abc-8185-47bc11aef59e Details

    Revised: 11/2022