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    NDC 27281-0039-64 VIVACITY 2; 3; 2; 2; 6; 3; 200; 6; 6; 8; 30; 200 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL Details

    VIVACITY 2; 3; 2; 2; 6; 3; 200; 6; 6; 8; 30; 200 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL

    VIVACITY is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Sunway Biotech LLC. The primary component is ALFALFA; ARNICA MONTANA; ASIAN GINSENG; AVENA SATIVA FLOWERING TOP; CERVUS ELAPHUS HORN OIL; GALIUM APARINE; HYPERICUM PERFORATUM; PORK LIVER; SACCHAROMYCES CEREVISIAE RNA; SUS SCROFA PITUITARY GLAND; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS.

    Product Information

    NDC 27281-0039
    Product ID 27281-039_d44c243b-ca3d-fee5-e053-2a95a90ace90
    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 VIVACITY
    Proprietary Name Suffix n/a
    Non-Proprietary Name Alfalfa, Arnica Montana, Avena Sativa, Galium Aparine, Hepar Suis, Hypericum Perforatum, Korean Ginseng, Oleum Animale, Pituitary Suis, Rhus Toxicodendron, RNA, Thuja occidentalis
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 2; 3; 2; 2; 6; 3; 200; 6; 6; 8; 30; 200
    Active Ingredient Units [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL
    Substance Name ALFALFA; ARNICA MONTANA; ASIAN GINSENG; AVENA SATIVA FLOWERING TOP; CERVUS ELAPHUS HORN OIL; GALIUM APARINE; HYPERICUM PERFORATUM; PORK LIVER; SACCHAROMYCES CEREVISIAE RNA; SUS SCROFA PITUITARY GLAND; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS
    Labeler Name Sunway Biotech LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 27281-0039-64 (27281003964)

    NDC Package Code 27281-039-64
    Billing NDC 27281003964
    Package 30 mL in 1 BOTTLE, SPRAY (27281-039-64)
    Marketing Start Date 2018-02-05
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL e0a6ee95-0cef-46c8-bd98-374ade4db6de Details

    Revised: 12/2021