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    NDC 70015-0650-02 OxyRub Max Pain Relief 25; 100 mg/g; mg/g Details

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

    OxyRub Max 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 70015-0650
    Product ID 70015-650_b8d79ecd-b1c0-461d-829b-2913dc48446f
    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 Max Pain Relief
    Proprietary Name Suffix Cream, 2oz
    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 70015-0650-02 (70015065002)

    NDC Package Code 70015-650-02
    Billing NDC 70015065002
    Package 1 TUBE in 1 CARTON (70015-650-02) / 57 g in 1 TUBE
    Marketing Start Date 2017-06-01
    NDC Exclude Flag N
    Pricing Information N/A
    << 70015-0645-04 70015-0655-04 >>

    Contents

    Standard Product Labeling (SPL)/Prescribing Information SPL 6fea637f-bf6f-455f-b3d0-416bca1b811d Details

    Revised: 5/2017
    Document Id: b8d79ecd-b1c0-461d-829b-2913dc48446f
    Set id: 6fea637f-bf6f-455f-b3d0-416bca1b811d
    Version: 1
    Effective Time: 20170502