rolaids ultra strength 1200

Generic: calcium carbonate, magnesium hydroxide

Labeler: the procter & gamble manufacturing company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name rolaids ultra strength 1200
Generic Name calcium carbonate, magnesium hydroxide
Labeler the procter & gamble manufacturing company
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

calcium carbonate 1000 mg/1, magnesium hydroxide 200 mg/1

Manufacturer
THE PROCTER & GAMBLE MANUFACTURING COMPANY

Identifiers & Regulatory

Product NDC 84126-325
Product ID 84126-325_44fa9bad-243b-6eb9-e063-6394a90a0757
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2024-12-09

Pharmacologic Class

Classes
blood coagulation factor [epc] calcium [cs] calculi dissolution agent [epc] cations divalent [cs] increased coagulation factor activity [pe] 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] phosphate binder [epc] phosphate chelating activity [moa] stimulation large intestine fluid/electrolyte secretion [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84126325
Hyphenated Format 84126-325

Supplemental Identifiers

RxCUI
1438105 1438107
UPC
0720112004535
UNII
H0G9379FGK NBZ3QY004S

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 rolaids ultra strength 1200 (source: ndc)
Generic Name calcium carbonate, magnesium hydroxide (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
  • 200 mg/1
source: ndc
Packaging
  • 10 TABLET, CHEWABLE in 1 PACKAGE (84126-325-10)
  • 72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (84126-325-72)
source: ndc

Packages (2)

Ingredients (2)

calcium carbonate (1000 mg/1) magnesium hydroxide (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "44fa9bad-243b-6eb9-e063-6394a90a0757", "openfda": {"upc": ["0720112004535"], "unii": ["H0G9379FGK", "NBZ3QY004S"], "rxcui": ["1438105", "1438107"], "spl_set_id": ["28d9897d-46bf-d206-e063-6394a90a2b27"], "manufacturer_name": ["THE PROCTER & GAMBLE MANUFACTURING COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, CHEWABLE in 1 PACKAGE (84126-325-10)", "package_ndc": "84126-325-10", "marketing_start_date": "20241209"}, {"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (84126-325-72)", "package_ndc": "84126-325-72", "marketing_start_date": "20241209"}], "brand_name": "Rolaids ULTRA STRENGTH 1200", "product_id": "84126-325_44fa9bad-243b-6eb9-e063-6394a90a0757", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Calculi Dissolution Agent [EPC]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "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]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "84126-325", "generic_name": "Calcium Carbonate, Magnesium Hydroxide", "labeler_name": "THE PROCTER & GAMBLE MANUFACTURING COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Rolaids ULTRA STRENGTH 1200", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "200 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241209", "listing_expiration_date": "20261231"}