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CHERRY ANTACID

Medically reviewed on Oct 25, 2016

Dosage form: tablet, chewable
Ingredients: CALCIUM CARBONATE 4201
Labeler: ADVANCED FIRST AID, INC.
NDC Code: 67060-304

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.

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 asdirected by a doctor.

Children under 12 years: Consult a doctor.

Inactive Ingredients: corn starch, FD&C Red #40, flavor, magnesium stearate, silicon dioxide, starch and sucrose.

CHERRY ANTACID 
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67060-304
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (CARBONATE ION) CALCIUM CARBONATE420 
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN 
FD&C RED NO. 40 
SUCROSE 
MAGNESIUM STEARATE 
SILICON DIOXIDE 
CHERRY 
Product Characteristics
Colorpink (ROSE PINK) Scoreno score
ShapeROUNDSize12mm
FlavorCHERRYImprint CodeFR8
Contains    
Packaging
#Item CodePackage Description
1NDC:67060-304-68100 PACKET in 1 CARTON
12 TABLET, CHEWABLE in 1 PACKET
2NDC:67060-304-67250 PACKET in 1 CARTON
22 TABLET, CHEWABLE in 1 PACKET
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/FEIOperations
ULTRA SEAL CORPORATION085752004pack(67060-304)
Establishment
NameAddressID/FEIOperations
ULTRA TAB LABORATORIES, INC.151051757manufacture(67060-304)

 
ADVANCED FIRST AID, INC.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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