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    NDC 50804-0619-12 MAXIMUM STRENGTH ANTACID AND GASRELIEF 800; 80; 800 mg/10mL; mg/10mL; mg/10mL Details

    MAXIMUM STRENGTH ANTACID AND GASRELIEF 800; 80; 800 mg/10mL; mg/10mL; mg/10mL

    MAXIMUM STRENGTH ANTACID AND GASRELIEF is a ORAL SUSPENSION in the HUMAN OTC DRUG category. It is labeled and distributed by GOODSENSE. The primary component is ALUMINUM HYDROXIDE; DIMETHICONE; MAGNESIUM HYDROXIDE.

    Product Information

    NDC 50804-0619
    Product ID 50804-619_0993d17e-73ca-48fd-e063-6294a90abc13
    Associated GPIs 48991003101835
    GCN Sequence Number 002706
    GCN Sequence Number Description mag hydrox/aluminum hyd/simeth ORAL SUSP 400-400-40 ORAL
    HIC3 D4B
    HIC3 Description ANTACIDS
    GCN 63915
    HICL Sequence Number 001168
    HICL Sequence Number Description MAGNESIUM HYDROXIDE/ALUMINUM HYDROXIDE/SIMETHICONE
    Brand/Generic Generic
    Proprietary Name MAXIMUM STRENGTH ANTACID AND GASRELIEF
    Proprietary Name Suffix n/a
    Non-Proprietary Name aluminum hydroxide, magnesium hydroxide, dimethicone
    Product Type HUMAN OTC DRUG
    Dosage Form SUSPENSION
    Route ORAL
    Active Ingredient Strength 800; 80; 800
    Active Ingredient Units mg/10mL; mg/10mL; mg/10mL
    Substance Name ALUMINUM HYDROXIDE; DIMETHICONE; MAGNESIUM HYDROXIDE
    Labeler Name GOODSENSE
    Pharmaceutical Class Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M001
    Listing Certified Through 2024-12-31

    Package

    NDC 50804-0619-12 (50804061912)

    NDC Package Code 50804-619-12
    Billing NDC 50804061912
    Package 355 mL in 1 BOTTLE (50804-619-12)
    Marketing Start Date 2020-07-01
    NDC Exclude Flag N
    Pricing Information N/A