antacid

Generic: aluminum hydroxide, magnesium hydroxide, simethicone

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name antacid
Generic Name aluminum hydroxide, magnesium hydroxide, simethicone
Labeler preferred pharmaceuticals inc.
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

aluminum hydroxide 400 mg/10mL, dimethicone, unspecified 40 mg/10mL, magnesium hydroxide 400 mg/10mL

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8506
Product ID 68788-8506_9370f05c-b940-4db0-abc1-c249264d6008
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number part331
Listing Expiration 2026-12-31
Marketing Start 2021-06-02

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] skin barrier activity [pe] stimulation large intestine fluid/electrolyte secretion [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888506
Hyphenated Format 68788-8506

Supplemental Identifiers

RxCUI
307746
UNII
5QB0T2IUN0 92RU3N3Y1O NBZ3QY004S

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 (source: ndc)
Generic Name aluminum hydroxide, magnesium hydroxide, simethicone (source: ndc)
Application Number part331 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/10mL
  • 40 mg/10mL
source: ndc
Packaging
  • 355 mL in 1 BOTTLE (68788-8506-3)
source: ndc

Packages (1)

Ingredients (3)

aluminum hydroxide (400 mg/10mL) dimethicone, unspecified (40 mg/10mL) magnesium hydroxide (400 mg/10mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9370f05c-b940-4db0-abc1-c249264d6008", "openfda": {"unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["307746"], "spl_set_id": ["a96496ff-4b35-4ebe-a6e4-bcfa48fb1341"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (68788-8506-3)", "package_ndc": "68788-8506-3", "marketing_start_date": "20230815"}], "brand_name": "Antacid", "product_id": "68788-8506_9370f05c-b940-4db0-abc1-c249264d6008", "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": "68788-8506", "generic_name": "aluminum hydroxide, magnesium hydroxide, simethicone", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antacid", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "400 mg/10mL"}, {"name": "DIMETHICONE, UNSPECIFIED", "strength": "40 mg/10mL"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "400 mg/10mL"}], "application_number": "part331", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210602", "listing_expiration_date": "20261231"}