Package 69842-619-12

Brand: maximum strength antacid

Generic: aluminum hydroxide, magnesium hydroxide, dimethicone
NDC Package

Package Facts

Identity

Package NDC 69842-619-12
Digits Only 6984261912
Product NDC 69842-619
Description

355 mL in 1 BOTTLE (69842-619-12)

Marketing

Marketing Status
Marketed Since 2020-09-01
Brand maximum strength antacid
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": "3580a6e2-1602-56a1-e063-6294a90af8f2", "openfda": {"nui": ["N0000010282"], "unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["237870"], "spl_set_id": ["af71e02d-e7c7-f925-e053-2995a90a0861"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (69842-619-12)", "package_ndc": "69842-619-12", "marketing_start_date": "20200901"}], "brand_name": "MAXIMUM STRENGTH ANTACID", "product_id": "69842-619_3580a6e2-1602-56a1-e063-6294a90af8f2", "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": "69842-619", "generic_name": "aluminum hydroxide, magnesium hydroxide, dimethicone", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MAXIMUM STRENGTH ANTACID", "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": "20200901", "listing_expiration_date": "20261231"}