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    NDC 69517-0109-50 All Day Pain Relief 220 mg/1 Details

    All Day Pain Relief 220 mg/1

    All Day Pain Relief is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by HealthLife of USA LLC. The primary component is NAPROXEN SODIUM.

    Product Information

    NDC 69517-0109
    Product ID 69517-109_046b91ed-d78b-42c0-b822-77fcbdeff84b
    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 All Day Pain Relief
    Proprietary Name Suffix n/a
    Non-Proprietary Name Naproxen Sodium Tablets, 220 mg
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 220
    Active Ingredient Units mg/1
    Substance Name NAPROXEN SODIUM
    Labeler Name HealthLife of USA LLC
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA091353
    Listing Certified Through 2024-12-31

    Package

    NDC 69517-0109-50 (69517010950)

    NDC Package Code 69517-109-50
    Billing NDC 69517010950
    Package 50 POUCH in 1 BOX (69517-109-50) / 2 TABLET in 1 POUCH
    Marketing Start Date 2016-04-07
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 7b0cb91e-5465-40ef-9f82-919f7d984f17 Details

    Revised: 6/2017