regular strength antacid

Generic: aluminum hydroxide, magnesium hydroxide, dimethicone

Labeler: chain drug marketing association
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 chain drug marketing association
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

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

Manufacturer
Chain Drug Marketing Association

Identifiers & Regulatory

Product NDC 63868-712
Product ID 63868-712_097f861d-60dc-700d-e063-6294a90afc78
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2014-03-01

Pharmacologic Class

Physiologic Effect
skin barrier activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63868712
Hyphenated Format 63868-712

Supplemental Identifiers

RxCUI
307746
UPC
0635515901230
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 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 (63868-712-57)
source: ndc

Packages (1)

63868-712-57 355 mL in 1 BOTTLE (63868-712-57)

Ingredients (3)

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

Linked Drug Pages (1)

REGULAR STRENGTH ANTACID ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "097f861d-60dc-700d-e063-6294a90afc78", "openfda": {"nui": ["N0000010282"], "upc": ["0635515901230"], "unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["307746"], "spl_set_id": ["9f410b3a-5579-4fae-84b1-5cd35563451e"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["Chain Drug Marketing Association"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (63868-712-57)", "package_ndc": "63868-712-57", "marketing_start_date": "20180801"}], "brand_name": "REGULAR STRENGTH ANTACID", "product_id": "63868-712_097f861d-60dc-700d-e063-6294a90afc78", "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": "63868-712", "generic_name": "aluminum hydroxide, magnesium hydroxide, dimethicone", "labeler_name": "Chain Drug Marketing Association", "product_type": "HUMAN OTC DRUG", "brand_name_base": "REGULAR STRENGTH 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": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140301", "listing_expiration_date": "20261231"}