Trial Antacid

Manufacturer
Cintas Corporation | Ultra Seal Corporation | Ultratab Laboratories, Inc.
Effective date
2021-01-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:57:51

Label at a glance#

ProductTrial Antacid
Active ingredientCALCIUM CARBONATE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient (in each tablet)  Calcium Carbonate-420 mg

OTC - PURPOSE SECTION

Purpose-Antacid

INDICATIONS & USAGE SECTION

Uses relieves:
■ heartburn
■ acid indigestion
■ sour stomach
■ upset stomach due to these symptoms

DOSAGE & ADMINISTRATION SECTION

Directions

  • chew 2 to 4 tablets. Repeat hourly if symptoms return.
  • do not take more than 18 tablets in 24 hours
  • do not use the maximum dosage more than 2 weeks

WARNINGS SECTION

Warnings
Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interfere
with certain prescription drugs

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding baby, ask a health professional  
before use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. In case of overdose,  
get medical help or contact a Poison Control Center right away.  
Prompt medical attention is critical for adults as well as for  
children even if you do not notice any signs or symptoms.

INACTIVE INGREDIENT SECTION

nactive ingredients
acacia*, cornstarch*, magnesium stearate, silica*, sorbitol, mint flavor, stearic acid* *contains one or more of these ingredients

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MM1Trial 250 BoxTrial 250 Box Trial 250 BoxTrial 250 Box Trial 250 BoxTrial 250 Box1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42961-04542961-045-01, 42961-045-02, 42961-045-03, 42961-045-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
2c901c2f-4e99-4a44-958d-7f66ee5574d5af3b6297-b3e4-461b-bca3-06dcd524e9cb2023-01-27WarningsExact identifier
spl set id: af3b6297-b3e4-461b-bca3-06dcd524e9cb

Reported adverse events (FAERS/openFDA)#

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