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    NDC 73501-0500-90 Tuvivex 40 mg/mL Details

    Tuvivex 40 mg/mL

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

    Product Information

    NDC 73501-0500
    Product ID 73501-500_8bbb6c64-f7a9-42d1-809e-d0883ac0f6e3
    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 Tuvivex
    Proprietary Name Suffix n/a
    Non-Proprietary Name MENTHOL, UNSPECIFIED FORM
    Product Type HUMAN OTC DRUG
    Dosage Form GEL
    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 73501-0500-90 (73501050090)

    NDC Package Code 73501-500-90
    Billing NDC 73501050090
    Package 90 mL in 1 BOTTLE, WITH APPLICATOR (73501-500-90)
    Marketing Start Date 2020-02-10
    NDC Exclude Flag N
    Pricing Information N/A
    << 73499-0001-03 73501-0501-10 >>

    Contents

    Standard Product Labeling (SPL)/Prescribing Information SPL 3b1f601d-58df-4429-b65e-bbc52d4711c3 Details

    Revised: 1/2022
    Document Id: 8bbb6c64-f7a9-42d1-809e-d0883ac0f6e3
    Set id: 3b1f601d-58df-4429-b65e-bbc52d4711c3
    Version: 2
    Effective Time: 20220127