geri-lanta antacid

Generic: aluminum hydroxide, magnesium hydroxide, dimethicone

Labeler: a-s medication solutions
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name geri-lanta antacid
Generic Name aluminum hydroxide, magnesium hydroxide, dimethicone
Labeler a-s medication solutions
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

aluminum hydroxide 200 mg/5mL, dimethicone 20 mg/5mL, magnesium hydroxide 200 mg/5mL

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4259
Product ID 50090-4259_34425db4-6600-452f-bcd7-c1291037c6e6
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH FINAL
Application Number part331
Listing Expiration 2026-12-31
Marketing Start 2000-01-01

Pharmacologic Class

Physiologic Effect
skin barrier activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500904259
Hyphenated Format 50090-4259

Supplemental Identifiers

RxCUI
307746
UNII
5QB0T2IUN0 92RU3N3Y1O NBZ3QY004S
NUI
N0000010282

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 geri-lanta antacid (source: ndc)
Generic Name aluminum hydroxide, magnesium hydroxide, dimethicone (source: ndc)
Application Number part331 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/5mL
  • 20 mg/5mL
source: ndc
Packaging
  • 355 mL in 1 BOTTLE (50090-4259-0)
source: ndc

Packages (1)

Ingredients (3)

aluminum hydroxide (200 mg/5mL) dimethicone (20 mg/5mL) magnesium hydroxide (200 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "34425db4-6600-452f-bcd7-c1291037c6e6", "openfda": {"nui": ["N0000010282"], "unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["307746"], "spl_set_id": ["3b13e528-b2e8-46c1-a3f9-e2e07f637cb8"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (50090-4259-0)", "package_ndc": "50090-4259-0", "marketing_start_date": "20190410"}], "brand_name": "GERI-LANTA ANTACID", "product_id": "50090-4259_34425db4-6600-452f-bcd7-c1291037c6e6", "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": "50090-4259", "generic_name": "aluminum hydroxide, magnesium hydroxide, dimethicone", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GERI-LANTA ANTACID", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "200 mg/5mL"}, {"name": "DIMETHICONE", "strength": "20 mg/5mL"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "200 mg/5mL"}], "application_number": "part331", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20000101", "listing_expiration_date": "20261231"}