69842-271 NDC - ULTRA STRENGTH ANTACID ASSORTED BERRIES (CALCIUM CARBONATE)

Drug Information

  • Product NDC: 69842-271
  • Proprietary Name: Ultra Strength Antacid Assorted Berries
  • Non Proprietary Name: Calcium carbonate
  • Active Ingredient(s): 1000 mg/1 CALCIUM CARBONATE
  • Administration Route(s): ORAL
  • Dosage Form(s): TABLET, CHEWABLE
  • Pharmacy Class(es): Blood Coagulation Factor [EPC]; Calcium [CS]; Cations; Divalent [CS]; Increased Coagulation Factor Activity [PE]

Labeler Information

Field Name Field Value
Labeler Name: CVS
Product Type: HUMAN OTC DRUG
FDA Application Number: part331
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:12/9/2011

Package Information

No. Package Code Package Description Billing Unit
169842-271-6872 TABLET, CHEWABLE in 1 BOTTLE (69842-271-68)
269842-271-75160 TABLET, CHEWABLE in 1 BOTTLE (69842-271-75)

NDC Record

Field Name Field Value Definition
PRODUCT NDC69842-271The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEUltra Strength Antacid Assorted BerriesThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECalcium carbonateThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLET, CHEWABLEThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE12/9/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERpart331Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
LABELER NAMECVSThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
SUBSTANCE NAMECALCIUM CARBONATEThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
ACTIVE NUMERATOR STRENGTH1000The translation of the dosage form Code submitted by the firm.
ACTIVE INGRED UNITmg/1The translation of the route code submitted by the firm, indicating route of administration.
PHARM CLASSESBlood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]This is the date that the labeler indicates was the start of its marketing of the drug product.

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This page was last updated on: 12/6/2025

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