maximum strength antacid

Generic: aluminum hydroxide, magnesium hydroxide, simethicone

Labeler: cardinal health
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name maximum strength antacid
Generic Name aluminum hydroxide, magnesium hydroxide, simethicone
Labeler cardinal health
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

aluminum hydroxide 400 mg/5mL, dimethicone 40 mg/5mL, magnesium hydroxide 400 mg/5mL

Manufacturer
CARDINAL HEALTH

Identifiers & Regulatory

Product NDC 70000-0422
Product ID 70000-0422_09939b31-cbee-6536-e063-6394a90ae969
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2019-01-01

Pharmacologic Class

Physiologic Effect
skin barrier activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 700000422
Hyphenated Format 70000-0422

Supplemental Identifiers

RxCUI
237870
UNII
5QB0T2IUN0 92RU3N3Y1O NBZ3QY004S
NUI
N0000010282

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 maximum strength antacid (source: ndc)
Generic Name aluminum hydroxide, magnesium hydroxide, simethicone (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/5mL
  • 40 mg/5mL
source: ndc
Packaging
  • 355 mL in 1 BOTTLE (70000-0422-1)
source: ndc

Packages (1)

Ingredients (3)

aluminum hydroxide (400 mg/5mL) dimethicone (40 mg/5mL) magnesium hydroxide (400 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09939b31-cbee-6536-e063-6394a90ae969", "openfda": {"nui": ["N0000010282"], "unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["237870"], "spl_set_id": ["7ee3618a-43c8-2ccc-e053-2a91aa0a8115"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["CARDINAL HEALTH"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (70000-0422-1)", "package_ndc": "70000-0422-1", "marketing_start_date": "20190101"}], "brand_name": "MAXIMUM STRENGTH ANTACID", "product_id": "70000-0422_09939b31-cbee-6536-e063-6394a90ae969", "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": "70000-0422", "generic_name": "aluminum hydroxide, magnesium hydroxide, simethicone", "labeler_name": "CARDINAL HEALTH", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MAXIMUM STRENGTH ANTACID", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "400 mg/5mL"}, {"name": "DIMETHICONE", "strength": "40 mg/5mL"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "400 mg/5mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190101", "listing_expiration_date": "20261231"}