Package 50804-619-12
Brand: maximum strength antacid and gasrelief
Generic: aluminum hydroxide, magnesium hydroxide, dimethiconePackage Facts
Identity
Package NDC
50804-619-12
Digits Only
5080461912
Product NDC
50804-619
Description
355 mL in 1 BOTTLE (50804-619-12)
Marketing
Marketing Status
Brand
maximum strength antacid and gasrelief
Generic
aluminum hydroxide, magnesium hydroxide, dimethicone
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0993d17e-73ca-48fd-e063-6294a90abc13", "openfda": {"nui": ["N0000010282"], "unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["237870"], "spl_set_id": ["a9654a96-9bfd-60ea-e053-2995a90ae38d"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["GOODSENSE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (50804-619-12)", "package_ndc": "50804-619-12", "marketing_start_date": "20200701"}], "brand_name": "MAXIMUM STRENGTH ANTACID AND GASRELIEF", "product_id": "50804-619_0993d17e-73ca-48fd-e063-6294a90abc13", "dosage_form": "SUSPENSION", "pharm_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 [MoA]", "Osmotic Laxative [EPC]", "Skin Barrier Activity [PE]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "50804-619", "generic_name": "aluminum hydroxide, magnesium hydroxide, dimethicone", "labeler_name": "GOODSENSE", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MAXIMUM STRENGTH ANTACID AND GASRELIEF", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "800 mg/10mL"}, {"name": "DIMETHICONE", "strength": "80 mg/10mL"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "800 mg/10mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}