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    NDC 43742-2090-01 REFL HS 6; 6; 10; 8; 8; 6; 6; 6; 6; 6; 6; 30; 6; 6; 8; 6; 8; 8; 12; 8; 8 [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details

    REFL HS 6; 6; 10; 8; 8; 6; 6; 6; 6; 6; 6; 30; 6; 6; 8; 6; 8; 8; 12; 8; 8 [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

    REFL HS is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is ADENOSINE TRIPHOSPHATE DISODIUM; ANHYDROUS CITRIC ACID; CENTAURIUM ERYTHRAEA; COENZYME A; COUMARIN; FORMIC ACID; HYDROCHLORIC ACID; IPECAC; LACTIC ACID, L-; NADIDE; OREGANO; PROTEUS INCONSTANS; ROBINIA PSEUDOACACIA BARK; SILVER NITRATE; STRYCHNOS NUX-VOMI.

    Product Information

    NDC 43742-2090
    Product ID 43742-2090_2bd661e9-dacf-414c-86b4-580ff4236694
    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 REFL HS
    Proprietary Name Suffix n/a
    Non-Proprietary Name Adenosinum Triphosphoricum Dinatrum, Nadidum, Argentum Nitricum, Ipecacuanha, Robinia Pseudoacacia, Sulphur, Origanum Vulgare, Duodenum (Suis), Esophagus (Suis), Funiculus Umbilicalis Suis, Stomach (Suis), Nux Vomica, Coumarinum, Erythraea Centaurium, Pan
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 6; 6; 10; 8; 8; 6; 6; 6; 6; 6; 6; 30; 6; 6; 8; 6; 8; 8; 12; 8; 8
    Active Ingredient Units [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
    Substance Name ADENOSINE TRIPHOSPHATE DISODIUM; ANHYDROUS CITRIC ACID; CENTAURIUM ERYTHRAEA; COENZYME A; COUMARIN; FORMIC ACID; HYDROCHLORIC ACID; IPECAC; LACTIC ACID, L-; NADIDE; OREGANO; PROTEUS INCONSTANS; ROBINIA PSEUDOACACIA BARK; SILVER NITRATE; STRYCHNOS NUX-VOMI
    Labeler Name Deseret Biologicals, Inc.
    Pharmaceutical Class Acidifying Activity [MoA], Allergens [CS], Allergens [CS], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Decreased Coagulation Factor Activity [PE], Dieta
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 43742-2090-01 (43742209001)

    NDC Package Code 43742-2090-1
    Billing NDC 43742209001
    Package 30 mL in 1 BOTTLE, DROPPER (43742-2090-1)
    Marketing Start Date 2023-07-14
    NDC Exclude Flag N
    Pricing Information N/A