ULINE ANTACID- calcium carbonate tablet, chewable 
Uline

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Uline Antacid

Drug Facts

Active ingredient (in each tablet)

Calcium Carbonate 420 mg

Purpose

Antacid

Uses

relieves

Warnings

Do not use

doctor

Ask a doctor or pharmacist before use if you

When using this product

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

Keep out of the reach of children.

Directions

Adults and children: (12 years and older) Chew 2 tablets every 2 - 3 hours as symptoms occur, repeat hourly if needed. Do not exceed 19 tablets in 24 hours.

Children under 12 years: Ask a doctor

Other information

Inactive ingredients

aspartame, croscarmellose sodium, magnesium stearate, maltodextrin, mint flavor, sorbitol

Questions or comments? 1-800-295-5510

ULINE

ANTACID

Tamper evident sealed packets:

Do not use if packet is open or torn.

Pull to Open

Calcium Carbonate 420 mg

• Do not swallow tablets whole

50 Packets

2 Tablets Each

Uline Antacid rev 4-13-21 Label

ULINE

ANTACID

Tamper evident sealed packets:

Do not use if packet is open or torn.

ANTACID

Pull to Open

Calcium Carbonate 420 mg

• Do not swallow tablets whole

50 Packets

2 Tablets Each

101R S-18596BX 3-2-23

ULINE ANTACID 
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69790-089
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE420 mg
Inactive Ingredients
Ingredient NameStrength
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
SUCROSE (UNII: C151H8M554)  
ACACIA (UNII: 5C5403N26O)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize12mm
FlavorMINTImprint Code FR;8
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69790-089-3350 in 1 BOX10/07/201903/01/2021
12 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00110/07/201903/01/2021
ULINE ANTACID 
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69790-820
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE420 mg
Inactive Ingredients
Ingredient NameStrength
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
SORBITOL (UNII: 506T60A25R)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize11mm
FlavorImprint Code AZ;036
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69790-820-3350 in 1 BOX10/07/2019
12 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00110/07/2019
Labeler - Uline (039612668)
Registrant - Unifirst First Aid Corporation (832947092)
Establishment
NameAddressID/FEIBusiness Operations
Prestige Packaging080667761pack(69790-089, 69790-820)
Establishment
NameAddressID/FEIBusiness Operations
Medique Products086911794pack(69790-820, 69790-089)

Revised: 1/2024
Document Id: 0fd919c9-d3a8-0d0e-e063-6394a90a13ad
Set id: 9014f295-e816-9bcd-e053-2a95a90ae103
Version: 8
Effective Time: 20240126
 
Uline