regular strength antacid

Generic: aluminum hydroxide, magnesium hydroxide, dimethicone

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

Drug Facts

Product Profile

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

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

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7841
Product ID 68788-7841_e03bb6b7-50d1-4949-9620-f7109c4e816b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2021-01-19

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 687887841
Hyphenated Format 68788-7841

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

Resolved Composition

Strengths
  • 200 mg/5mL
  • 20 mg/5mL
source: ndc
Packaging
  • 355 mL in 1 BOTTLE (68788-7841-3)
source: ndc

Packages (1)

Ingredients (3)

aluminum hydroxide (200 mg/5mL) dimethicone, unspecified (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": "e03bb6b7-50d1-4949-9620-f7109c4e816b", "openfda": {"unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["307746"], "spl_set_id": ["ad3e7ebe-f2a9-4305-b370-59785f5396c8"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (68788-7841-3)", "package_ndc": "68788-7841-3", "marketing_start_date": "20210119"}], "brand_name": "REGULAR STRENGTH ANTACID", "product_id": "68788-7841_e03bb6b7-50d1-4949-9620-f7109c4e816b", "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": "68788-7841", "generic_name": "aluminum hydroxide, magnesium hydroxide, dimethicone", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "REGULAR STRENGTH ANTACID", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "200 mg/5mL"}, {"name": "DIMETHICONE, UNSPECIFIED", "strength": "20 mg/5mL"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "200 mg/5mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210119", "listing_expiration_date": "20261231"}