mag-al liquid

Generic: aluminum hydroxide and magnesium hydroxide

Labeler: pai holdings, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mag-al liquid
Generic Name aluminum hydroxide and magnesium hydroxide
Labeler pai holdings, llc
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

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

Manufacturer
PAI Holdings, LLC

Identifiers & Regulatory

Product NDC 0121-1760
Product ID 0121-1760_23f8e329-625d-1e98-e063-6394a90a7df2
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2004-01-14

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 01211760
Hyphenated Format 0121-1760

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

Resolved Composition

Strengths
  • 200 mg/5mL
source: ndc
Packaging
  • 10 TRAY in 1 CASE (0121-1760-30) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE
source: ndc

Packages (1)

0121-1760-30 10 TRAY in 1 CASE (0121-1760-30) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE

Ingredients (2)

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

Linked Drug Pages (1)

Mag-AL Liquid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "23f8e329-625d-1e98-e063-6394a90a7df2", "openfda": {"unii": ["5QB0T2IUN0", "NBZ3QY004S"], "rxcui": ["243463"], "spl_set_id": ["b1f2d137-f5f7-4800-a1df-ef5d25544bc9"], "manufacturer_name": ["PAI Holdings, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (0121-1760-30)  / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE", "package_ndc": "0121-1760-30", "marketing_start_date": "20040114"}], "brand_name": "Mag-AL Liquid", "product_id": "0121-1760_23f8e329-625d-1e98-e063-6394a90a7df2", "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": "0121-1760", "generic_name": "Aluminum Hydroxide and Magnesium Hydroxide", "labeler_name": "PAI Holdings, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mag-AL Liquid", "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": "20040114", "listing_expiration_date": "20261231"}