ultra strength antacid

Generic: calcium antacid

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

Drug Facts

Product Profile

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

calcium carbonate 1000 mg/1

Manufacturer
CVS

Identifiers & Regulatory

Product NDC 69842-171
Product ID 69842-171_ce8cfb77-e2d9-42a6-985c-534591993edb
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH FINAL
Application Number part331
Listing Expiration 2026-12-31
Marketing Start 2011-12-09

Pharmacologic Class

Classes
blood coagulation factor [epc] calcium [cs] cations divalent [cs] increased coagulation factor activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69842171
Hyphenated Format 69842-171

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 ultra strength antacid (source: ndc)
Generic Name calcium antacid (source: ndc)
Application Number part331 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 72 TABLET, CHEWABLE in 1 BOTTLE (69842-171-68)
  • 160 TABLET, CHEWABLE in 1 BOTTLE (69842-171-72)
source: ndc

Packages (2)

69842-171-68 72 TABLET, CHEWABLE in 1 BOTTLE (69842-171-68) 69842-171-72 160 TABLET, CHEWABLE in 1 BOTTLE (69842-171-72)

Ingredients (1)

calcium carbonate (1000 mg/1)

Linked Drug Pages (1)

Ultra Strength Antacid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ce8cfb77-e2d9-42a6-985c-534591993edb", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["51acc196-ab1f-49ea-8a59-f06309f1953b"], "manufacturer_name": ["CVS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (69842-171-68)", "package_ndc": "69842-171-68", "marketing_start_date": "20111209"}, {"sample": false, "description": "160 TABLET, CHEWABLE in 1 BOTTLE (69842-171-72)", "package_ndc": "69842-171-72", "marketing_start_date": "20111209"}], "brand_name": "Ultra Strength Antacid", "product_id": "69842-171_ce8cfb77-e2d9-42a6-985c-534591993edb", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]"], "product_ndc": "69842-171", "generic_name": "Calcium Antacid", "labeler_name": "CVS", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ultra Strength Antacid", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "part331", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20111209", "listing_expiration_date": "20261231"}