MINT ANTACID- calcium carbonate tablet, chewable 
ADVANCED FIRST AID, 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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ACTIVE INGREDIENT IN EACH TABLET- CALCIUM CARBONATE 420 MG

ANTACID

Uses:

for the relief of:

•heartburn • sour stomach • acid indigestion

Warnings:

Do not:

•Take more than 18 tablets in a 24 hour period, or use the maximum dosage of

this product for more than 2 weeks, except under the advice of a physician.

Stop use and ask a doctor if:

•You are currently taking any prescription drug. Antacids may react 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.

Directions:

Adults and children 12 years of age and older:  Take 2 tablets every 4 to

6 hours or as needed, do not exceed 18 tablets in 24 hours, or as directed by a doctor.

Children under 12 years: Consult a doctor.

Inactive Ingredients: acacia gum, flavor, magnesium stearate, maltodextrin, starch and sugar.

Mint Carton

MINT ANTACID 
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67060-303
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE420 
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
ACACIA (UNII: 5C5403N26O)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
Product Characteristics
Colorwhite (WHITE) Scoreno score
ShapeROUNDSize12mm
FlavorMINTImprint Code FR8
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67060-303-68100 in 1 CARTON04/07/2015
1NDC:67060-303-022 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33104/07/2015
Labeler - ADVANCED FIRST AID, INC. (114477180)
Registrant - ADVANCED FIRST AID, INC. (114477180)
Establishment
NameAddressID/FEIBusiness Operations
ULTRA SEAL CORPORATION085752004pack(67060-303)
Establishment
NameAddressID/FEIBusiness Operations
ULTRA TAB LABORATORIES, INC.151051757manufacture(67060-303)

Revised: 3/2019
Document Id: 8ebfe9e5-309f-446d-9107-b88bf733dcbb
Set id: 4989063a-7b6a-4e8a-8e97-29368d94dd0a
Version: 3
Effective Time: 20190313
 
ADVANCED FIRST AID, INC.