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    NDC 72850-0005-01 Decasilin 5.82; 17.12; 17.12; 22.95; 17.12; 17.12 1/1001; 1/1001; 1/1001; 1/1001; 1/1001; 1/1001 Details

    Decasilin 5.82; 17.12; 17.12; 22.95; 17.12; 17.12 1/1001; 1/1001; 1/1001; 1/1001; 1/1001; 1/1001

    Decasilin is a ORAL CAPSULE in the HUMAN OTC DRUG category. It is labeled and distributed by Chunwoo Pharmaceutical Co., Ltd.. The primary component is GINGER; JUJUBE FRUIT; LICORICE; PAEONIA LACTIFLORA ROOT; PLATYCODON GRANDIFLORUS ROOT; PONCIRUS TRIFOLIATA FRUIT.

    Product Information

    NDC 72850-0005
    Product ID 72850-0005_972ca92a-41a9-712a-e053-2995a90a4926
    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 Decasilin
    Proprietary Name Suffix n/a
    Non-Proprietary Name poncirus trifoliata fruit, peony root, platycodon root
    Product Type HUMAN OTC DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 5.82; 17.12; 17.12; 22.95; 17.12; 17.12
    Active Ingredient Units 1/1001; 1/1001; 1/1001; 1/1001; 1/1001; 1/1001
    Substance Name GINGER; JUJUBE FRUIT; LICORICE; PAEONIA LACTIFLORA ROOT; PLATYCODON GRANDIFLORUS ROOT; PONCIRUS TRIFOLIATA FRUIT
    Labeler Name Chunwoo Pharmaceutical Co., Ltd.
    Pharmaceutical Class Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
    DEA Schedule n/a
    Marketing Category UNAPPROVED DRUG OTHER
    Application Number n/a
    Listing Certified Through 2022-12-31

    Package

    NDC 72850-0005-01 (72850000501)

    NDC Package Code 72850-0005-1
    Billing NDC 72850000501
    Package 10 CAPSULE in 1 BLISTER PACK (72850-0005-1)
    Marketing Start Date 2019-10-19
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 970b0ada-66d3-74fc-e053-2a95a90aee83 Details

    Revised: 11/2019