TRIAL ANTACID- calcium carbonate tablet
Zee Medical Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

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

Purpose-Antacid

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

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

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

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.

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

MM1 Trial 250 Box 1

TRIAL ANTACID
calcium carbonate tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:35418-310
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D)	CALCIUM CARBONATE	420 mg

Ingredient Name	Strength
Inactive Ingredients
SORBITOL (UNII: 506T60A25R)
ACACIA (UNII: 5C5403N26O)
MAGNESIUM STEARATE (UNII: 70097M6I30)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STARCH, CORN (UNII: O8232NY3SJ)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color	white (snow white)	Score	no score
Shape	ROUND (ZEE;TL)	Size	13mm
Flavor	SPEARMINT (spearmint)	Imprint Code	ZEE;TL
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:35418-310-69	500 in 1 CARTON	06/12/2012	06/01/2023
1	NDC:35418-310-68	50 in 1 CARTON
1	NDC:35418-310-67	125 in 1 CARTON
1	NDC:35418-310-02	2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part331	06/12/2012	06/01/2023

Labeler - Zee Medical Inc (009645623)

Name	Address	ID/FEI	Business Operations
Establishment
Ultratab Laboratories, Inc.		151051757	manufacture(35418-310)

Revised: 1/2023

Document Id: f19c5d7f-48e7-d2c6-e053-2995a90a4255

Set id: a17b9b76-b932-4147-99b1-d3b1f42f175d

Version: 4

Effective Time: 20230106

Zee Medical Inc