Package 81033-006-01

Brand: kesin mag-al plus

Generic: aluminum and magnesium hydroxide w/simethicone suspension
NDC Package

Package Facts

Identity

Package NDC 81033-006-01
Digits Only 8103300601
Product NDC 81033-006
Description

100 CUP, UNIT-DOSE in 1 CASE (81033-006-01) / 30 mL in 1 CUP, UNIT-DOSE (81033-006-30)

Marketing

Marketing Status
Marketed Since 2025-11-05
Brand kesin mag-al plus
Generic aluminum and magnesium hydroxide w/simethicone suspension
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "436b6235-e384-d238-e063-6394a90a2818", "openfda": {"unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["307746"], "spl_set_id": ["436b622a-f028-df98-e063-6394a90a3eaa"], "manufacturer_name": ["Kesin Pharma Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (81033-006-01)  / 30 mL in 1 CUP, UNIT-DOSE (81033-006-30)", "package_ndc": "81033-006-01", "marketing_start_date": "20251105"}], "brand_name": "Kesin MAG-AL Plus", "product_id": "81033-006_436b6235-e384-d238-e063-6394a90a2818", "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": "81033-006", "generic_name": "Aluminum and Magnesium Hydroxide w/Simethicone Suspension", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kesin MAG-AL Plus", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "200 mg/5mL"}, {"name": "DIMETHICONE, UNSPECIFIED", "strength": "20 mg/5mL"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "200 mg/5mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251105", "listing_expiration_date": "20261231"}