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    NDC 69517-0131-10 SENNA-S 50; 8.6 mg/1; mg/1 Details

    SENNA-S 50; 8.6 mg/1; mg/1

    SENNA-S is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by HealthLife of USA LLC. The primary component is DOCUSATE SODIUM; SENNOSIDES.

    Product Information

    NDC 69517-0131
    Product ID 69517-131_083396b6-6a49-ffc7-e063-6294a90ad8e2
    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 SENNA-S
    Proprietary Name Suffix n/a
    Non-Proprietary Name Senna and Docusate Sodium Tablets, 8.6 mg and 50 mg
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 50; 8.6
    Active Ingredient Units mg/1; mg/1
    Substance Name DOCUSATE SODIUM; SENNOSIDES
    Labeler Name HealthLife of USA LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number 505G(a)(3)
    Listing Certified Through 2024-12-31

    Package

    NDC 69517-0131-10 (69517013110)

    NDC Package Code 69517-131-10
    Billing NDC 69517013110
    Package 1000 BOTTLE in 1 BOTTLE (69517-131-10) / 500 BOTTLE in 1 BOTTLE (69517-131-05) / 24 CARTON in 1 BOTTLE (69517-131-24) / 1 TABLET, COATED in 1 CARTON
    Marketing Start Date 2016-04-08
    NDC Exclude Flag N
    Pricing Information N/A