rolaids ultra strength mint

Generic: calcium carbonate and magnesium hydroxide

Labeler: chattem, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name rolaids ultra strength mint
Generic Name calcium carbonate and magnesium hydroxide
Labeler chattem, inc.
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

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

Manufacturer
Chattem, Inc.

Identifiers & Regulatory

Product NDC 41167-1003
Product ID 41167-1003_5a3751c1-7f0f-4dcf-93e9-8e0cff9116b1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2027-12-31
Marketing Start 2013-09-01

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 411671003
Hyphenated Format 41167-1003

Supplemental Identifiers

RxCUI
1438105 1438107
UPC
0041167100318
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 mint (source: ndc)
Generic Name calcium carbonate and 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
  • 72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (41167-1003-1)
  • 10 TABLET, CHEWABLE in 1 PACKAGE (41167-1003-4)
source: ndc

Packages (2)

41167-1003-1 72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (41167-1003-1) 41167-1003-4 10 TABLET, CHEWABLE in 1 PACKAGE (41167-1003-4)

Ingredients (2)

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

Linked Drug Pages (1)

Rolaids Ultra Strength Mint ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5a3751c1-7f0f-4dcf-93e9-8e0cff9116b1", "openfda": {"upc": ["0041167100318"], "unii": ["H0G9379FGK", "NBZ3QY004S"], "rxcui": ["1438105", "1438107"], "spl_set_id": ["8806c912-ab83-4f45-ac78-e826bb3143d4"], "manufacturer_name": ["Chattem, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (41167-1003-1)", "package_ndc": "41167-1003-1", "marketing_start_date": "20130901"}, {"sample": false, "description": "10 TABLET, CHEWABLE in 1 PACKAGE (41167-1003-4)", "package_ndc": "41167-1003-4", "marketing_start_date": "20130901"}], "brand_name": "Rolaids Ultra Strength Mint", "product_id": "41167-1003_5a3751c1-7f0f-4dcf-93e9-8e0cff9116b1", "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": "41167-1003", "generic_name": "Calcium carbonate and Magnesium hydroxide", "labeler_name": "Chattem, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Rolaids Ultra Strength Mint", "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": "20130901", "listing_expiration_date": "20271231"}