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    NDC 81183-0102-30 THE FLOWER REMEDY Get Up and Go 200; 5; 5; 5; 5; 5; 5; 5 [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL Details

    THE FLOWER REMEDY Get Up and Go 200; 5; 5; 5; 5; 5; 5; 5 [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL

    THE FLOWER REMEDY Get Up and Go is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by The Flower Remedy. The primary component is ACTIVATED CHARCOAL; BROMUS RAMOSUS FLOWER; CASTANEA SATIVA FLOWER; GENTIANELLA AMARELLA FLOWER; LARIX DECIDUA FLOWERING TOP; OLEA EUROPAEA FLOWER; QUERCUS ROBUR FLOWER; ULEX EUROPAEUS FLOWER.

    Product Information

    NDC 81183-0102
    Product ID 81183-102_78a8d075-f8eb-4cde-9242-a6510f0d1c03
    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 THE FLOWER REMEDY Get Up and Go
    Proprietary Name Suffix n/a
    Non-Proprietary Name Gentianella amarella, Ulex europaeus, Larix decidua, Quercus robur, Olea europaea, Castanea sativa, Bromus ramosus, Carbo Vegetabilis
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 200; 5; 5; 5; 5; 5; 5; 5
    Active Ingredient Units [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
    Substance Name ACTIVATED CHARCOAL; BROMUS RAMOSUS FLOWER; CASTANEA SATIVA FLOWER; GENTIANELLA AMARELLA FLOWER; LARIX DECIDUA FLOWERING TOP; OLEA EUROPAEA FLOWER; QUERCUS ROBUR FLOWER; ULEX EUROPAEUS FLOWER
    Labeler Name The Flower Remedy
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 81183-0102-30 (81183010230)

    NDC Package Code 81183-102-30
    Billing NDC 81183010230
    Package 30 mL in 1 BOTTLE, DROPPER (81183-102-30)
    Marketing Start Date 2021-04-26
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 52171aaa-8154-46c4-a807-7a7d209aa6cc Details

    Revised: 4/2021