ANTACID- calcium carbonate tablet 
Trifecta Pharmaceuticals USA LLC

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Antacid Calcium Carbonate Tablet, chewable

Active Ingredient (in each tablet)

Calcium Carbonate 420mg

Purpose

Antacid

Uses

Relieves

Directions

Chew 2 tablets every 2-3 hours or as symptoms occur, repeat hourly if needed.

Warnings

Ask a doctor or pharmacist before use if you

Keep out of reach of children

Keep out of reach of children

Other Information

Do not use if packet is open or torn

Tamper Evident

Chewable

Inactive Ingredients

Magnesium Stearate, Aspartame. Croscarmellose Sodium, Maltodextrin, mint flavor, sorbitol

Questions or Comments?

Call 1-888-296-9067

When using this product

Do not take more than 19 tablets in a 24 hour period or use the maximum dosage of this product for more than two weeks except under the advice and supervision of a doctor. If symptoms persist for more than two weeks, stop using this product and see a doctor.

Distributed By:

Distributed By:

Trifecta Pharmaceuticals USA®

Ft. Lauderdale, FL. 33301 USA

1-888-296-9067

*This product is not manufactured or distributed by GSK, owner of the registered trademark Tums®

Reorder No. 2016

CS 2016 Globe Antacid 50pk 031124 CDER

ANTACID 
calcium carbonate tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69396-142
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE420 mg
Inactive Ingredients
Ingredient NameStrength
ASPARTAME (UNII: Z0H242BBR1)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
SORBITOL (UNII: 506T60A25R)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
MINT (UNII: FV98Z8GITP)  
Product Characteristics
ColorwhiteScorescore with uneven pieces
ShapeROUNDSize11mm
FlavorMINTImprint Code AZ036
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69396-142-0150 in 1 BOX08/08/2023
12 in 1 PACKET; Type 0: Not a Combination Product
2NDC:69396-142-0510000 in 1 BAG08/08/2023
22 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00108/08/2023
Labeler - Trifecta Pharmaceuticals USA LLC (079424163)

Revised: 3/2024
Document Id: 14a7bb2e-96c5-6f6d-e063-6394a90a71f1
Set id: 14a7916e-5363-7f1b-e063-6294a90a20aa
Version: 1
Effective Time: 20240327
 
Trifecta Pharmaceuticals USA LLC