kesin mag-al

Generic: aluminum and magnesium hydroxide suspension

Labeler: kesin pharma corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name kesin mag-al
Generic Name aluminum and magnesium hydroxide suspension
Labeler kesin pharma corporation
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

aluminum hydroxide 200 mg/5mL, magnesium hydroxide 200 mg/5mL

Manufacturer
Kesin Pharma Corporation

Identifiers & Regulatory

Product NDC 81033-005
Product ID 81033-005_42df2224-eb9a-e3a5-e063-6394a90aa5c7
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2025-11-05

Pharmacologic Class

Classes
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] stimulation large intestine fluid/electrolyte secretion [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 81033005
Hyphenated Format 81033-005

Supplemental Identifiers

RxCUI
243463
UNII
5QB0T2IUN0 NBZ3QY004S

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name kesin mag-al (source: ndc)
Generic Name aluminum and magnesium hydroxide suspension (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/5mL
source: ndc
Packaging
  • 100 CUP, UNIT-DOSE in 1 CASE (81033-005-01) / 30 mL in 1 CUP, UNIT-DOSE (81033-005-30)
source: ndc

Packages (1)

81033-005-01 100 CUP, UNIT-DOSE in 1 CASE (81033-005-01) / 30 mL in 1 CUP, UNIT-DOSE (81033-005-30)

Ingredients (2)

aluminum hydroxide (200 mg/5mL) magnesium hydroxide (200 mg/5mL)

Linked Drug Pages (1)

Kesin MAG-AL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "42df2224-eb9a-e3a5-e063-6394a90aa5c7", "openfda": {"unii": ["5QB0T2IUN0", "NBZ3QY004S"], "rxcui": ["243463"], "spl_set_id": ["42df2198-14dc-da1c-e063-6394a90a1ae6"], "manufacturer_name": ["Kesin Pharma Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (81033-005-01)  / 30 mL in 1 CUP, UNIT-DOSE (81033-005-30)", "package_ndc": "81033-005-01", "marketing_start_date": "20251105"}], "brand_name": "Kesin MAG-AL", "product_id": "81033-005_42df2224-eb9a-e3a5-e063-6394a90aa5c7", "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]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "81033-005", "generic_name": "Aluminum and Magnesium Hydroxide Suspension", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kesin MAG-AL", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "200 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"}