cvs ultra strength

Generic: antacid tablets

Labeler: cvs
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name cvs ultra strength
Generic Name antacid tablets
Labeler cvs
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

calcium carbonate 1000 mg/1

Manufacturer
CVS

Identifiers & Regulatory

Product NDC 51316-031
Product ID 51316-031_4520d1c5-2b89-6314-e063-6294a90a661b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2021-08-06

Pharmacologic Class

Classes
blood coagulation factor [epc] calcium [cs] cations divalent [cs] increased coagulation factor activity [pe] phosphate binder [epc] phosphate chelating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51316031
Hyphenated Format 51316-031

Supplemental Identifiers

RxCUI
308892
UNII
H0G9379FGK

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 cvs ultra strength (source: ndc)
Generic Name antacid tablets (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 72 TABLET, CHEWABLE in 1 BOTTLE (51316-031-72)
source: ndc

Packages (1)

Ingredients (1)

calcium carbonate (1000 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4520d1c5-2b89-6314-e063-6294a90a661b", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["6108271a-4336-4f90-9765-9c3aea109488"], "manufacturer_name": ["CVS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (51316-031-72)", "package_ndc": "51316-031-72", "marketing_start_date": "20210806"}], "brand_name": "CVS Ultra Strength", "product_id": "51316-031_4520d1c5-2b89-6314-e063-6294a90a661b", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "51316-031", "generic_name": "Antacid Tablets", "labeler_name": "CVS", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CVS Ultra Strength", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210806", "listing_expiration_date": "20261231"}