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    NDC 70015-0655-04 OxyRub Pro Pain Relief 25; 100 mg/g; mg/g Details

    OxyRub Pro Pain Relief 25; 100 mg/g; mg/g

    OxyRub Pro Pain Relief is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by Healthy Directions, LLC. The primary component is MENTHOL; METHYL SALICYLATE.

    Product Information

    NDC 70015-0655
    Product ID 70015-655_d417edfb-86ce-4554-b1ce-ce126af62abb
    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 OxyRub Pro Pain Relief
    Proprietary Name Suffix Cream, 4oz
    Non-Proprietary Name Menthol, Methyl Salicylate
    Product Type HUMAN OTC DRUG
    Dosage Form CREAM
    Route TOPICAL
    Active Ingredient Strength 25; 100
    Active Ingredient Units mg/g; mg/g
    Substance Name MENTHOL; METHYL SALICYLATE
    Labeler Name Healthy Directions, LLC
    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 70015-0655-04 (70015065504)

    NDC Package Code 70015-655-04
    Billing NDC 70015065504
    Package 1 TUBE in 1 CARTON (70015-655-04) / 114 g in 1 TUBE
    Marketing Start Date 2017-09-01
    NDC Exclude Flag N
    Pricing Information N/A
    << 70015-0650-02 70015-0660-02 >>

    Contents

    Standard Product Labeling (SPL)/Prescribing Information SPL be26909d-afbb-4b89-a64a-fd130de223c7 Details

    Revised: 8/2017
    Document Id: d417edfb-86ce-4554-b1ce-ce126af62abb
    Set id: be26909d-afbb-4b89-a64a-fd130de223c7
    Version: 1
    Effective Time: 20170815