antacid and gasrelief

Generic: aluminum hydroxide, magnesium hydroxide, simethicone

Labeler: goodsense
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name antacid and gasrelief
Generic Name aluminum hydroxide, magnesium hydroxide, simethicone
Labeler goodsense
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

aluminum hydroxide 800 mg/10mL, dimethicone 80 mg/10mL, magnesium hydroxide 800 mg/10mL

Manufacturer
GOODSENSE

Identifiers & Regulatory

Product NDC 50804-638
Product ID 50804-638_099439f3-879b-7747-e063-6394a90a3706
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2020-07-01

Pharmacologic Class

Physiologic Effect
skin barrier activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50804638
Hyphenated Format 50804-638

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

Resolved Composition

Strengths
  • 800 mg/10mL
  • 80 mg/10mL
source: ndc
Packaging
  • 355 mL in 1 BOTTLE (50804-638-12)
source: ndc

Packages (1)

Ingredients (3)

aluminum hydroxide (800 mg/10mL) dimethicone (80 mg/10mL) magnesium hydroxide (800 mg/10mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "099439f3-879b-7747-e063-6394a90a3706", "openfda": {"nui": ["N0000010282"], "unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["237870"], "spl_set_id": ["a9654a96-9bf9-60ea-e053-2995a90ae38d"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["GOODSENSE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (50804-638-12)", "package_ndc": "50804-638-12", "marketing_start_date": "20200701"}], "brand_name": "ANTACID AND GASRELIEF", "product_id": "50804-638_099439f3-879b-7747-e063-6394a90a3706", "dosage_form": "LIQUID", "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": "50804-638", "generic_name": "aluminum hydroxide, magnesium hydroxide, simethicone", "labeler_name": "GOODSENSE", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ANTACID AND GASRELIEF", "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": "20200701", "listing_expiration_date": "20261231"}