Package 11822-3324-7
Brand: regular strength antacid and gas relief
Generic: aluminum hydroxide, magnesium hydroxide, dimethiconePackage Facts
Identity
Package NDC
11822-3324-7
Digits Only
1182233247
Product NDC
11822-3324
Description
355 mL in 1 BOTTLE (11822-3324-7)
Marketing
Marketing Status
Brand
regular strength antacid and gas relief
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": "43f66025-df58-06b3-e063-6294a90a6679", "openfda": {"nui": ["N0000010282"], "unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["307746"], "spl_set_id": ["602795f6-dbd2-1747-e053-2991aa0aa1ab"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["RITE AID PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (11822-3324-7)", "package_ndc": "11822-3324-7", "marketing_end_date": "20260731", "marketing_start_date": "20140401"}], "brand_name": "REGULAR STRENGTH ANTACID AND GAS RELIEF", "product_id": "11822-3324_43f66025-df58-06b3-e063-6294a90a6679", "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": "11822-3324", "generic_name": "aluminum hydroxide, magnesium hydroxide, dimethicone", "labeler_name": "RITE AID PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "REGULAR STRENGTH ANTACID AND GAS RELIEF", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "200 mg/5mL"}, {"name": "DIMETHICONE", "strength": "20 mg/5mL"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "200 mg/5mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260731", "marketing_start_date": "20140401"}