FDA.reportPublic FDA data

Cidatrine-TM

Manufacturer
Singular Dreamer Ltd.dba True Marker
Effective date
2023-11-06
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:21:50

Label at a glance#

ProductCidatrine-TM
Active ingredientCALCIUM CARBONATE, MAGNESIUM CARBONATE
Label structure8 sections

Indications and uses

relieves: heartburn sour stomach acid indigestion upset stomach associated with these symptoms

Dosage and administration

adults and children 12 years of age and over: take 3 to 4 tablets per day or as directed by a physician.

Label contents#

Full prescribing information#

Active ingredients (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Calcium Carbonate USP  975mg

Magnesium Carbonate USP  232mg

Purpose

OTC - PURPOSE SECTION

Antacid

Uses

INDICATIONS & USAGE SECTION

relieves:

  • heartburn
  • sour stomach
  • acid indigestion
  • upset stomach associated with these symptoms

Warnings

WARNINGS SECTION

Ask a doctor or pharmacist before use if you

  • are now taking a prescription drug. Antacids may interact with certain prescription drugs.

When using this product

  • do not take more than 8 tablets in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice or supervision of a physician.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 12 years of age and over: take 3 to 4 tablets per day or as directed by a physician.

Other information

SPL UNCLASSIFIED SECTION

  • each tablet contains: elemental Calcium 360mg and Magnesium 54mg.
  • do not use if seal is torn or missing.
  • store at room temperure. Keep the container tightly closed.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Modified cellulose gum, vegetable stearates, silicon dioxide. White Film Containing: Polyvinyl alchol, titanium dioxide, polyethelyne glycol, talc

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
83035-1480-9EA - Each83035-1480c04b6fe9-ea4c-491d-88dc-3853f775cc2f12023-03-13

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83035-148083035-1480-9

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERYL TRISTEARATEP6OCJ2551RIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT
TALC7SEV7J4R1UIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
POLYVINYL ALCOHOL, UNSPECIFIED532B59J990IACT
CROSCARMELLOSE SODIUMM28OL1HH48IACT
CALCIUM CARBONATEH0G9379FGKACTIM
MAGNESIUM CARBONATE0E53J927NAACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
097b6d9a-32e3-3266-e063-6294a90a2d96b49d7b45-399c-40d4-9b01-1dbc83955da52023-11-06WarningsExact identifier
spl id: 097b6d9a-32e3-3266-e063-6294a90a2d96
spl set id: b49d7b45-399c-40d4-9b01-1dbc83955da5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.