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    NDC 73501-0501-10 Tuvivex10 40 mg/mL Details

    Tuvivex10 40 mg/mL

    Tuvivex10 is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by Tuvive Therapeutics. The primary component is MENTHOL, UNSPECIFIED FORM.

    Product Information

    NDC 73501-0501
    Product ID 73501-501_17c2eaba-b3b5-406a-b9c7-8f4322d7f209
    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 Tuvivex10
    Proprietary Name Suffix n/a
    Non-Proprietary Name MENTHOL, UNSPECIFIED FORM
    Product Type HUMAN OTC DRUG
    Dosage Form CREAM
    Route TOPICAL
    Active Ingredient Strength 40
    Active Ingredient Units mg/mL
    Substance Name MENTHOL, UNSPECIFIED FORM
    Labeler Name Tuvive Therapeutics
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH NOT FINAL
    Application Number part348
    Listing Certified Through 2023-12-31

    Package

    NDC 73501-0501-10 (73501050110)

    NDC Package Code 73501-501-10
    Billing NDC 73501050110
    Package 100 mL in 1 BOTTLE, PUMP (73501-501-10)
    Marketing Start Date 2020-02-10
    NDC Exclude Flag N
    Pricing Information N/A
    << 73501-0500-90 73502-0286-15 >>

    Contents

    Standard Product Labeling (SPL)/Prescribing Information SPL 87396d87-c57d-44e2-a92c-66942430f047 Details

    Revised: 1/2022
    Document Id: 17c2eaba-b3b5-406a-b9c7-8f4322d7f209
    Set id: 87396d87-c57d-44e2-a92c-66942430f047
    Version: 2
    Effective Time: 20220127