ALKA SELTZER- calcium carbonate tablet, chewable 
BestCo 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.

----------

Calcium carbonate 750 mg

Active ingredient (in each chewable tablet)

Calcium carbonate 750 mg

Purpose

Antacid

Uses for the relief of:

Warnings

Do not useif you have ever had an allergic reaction to this product or any of its ingredients

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

When using this product

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

Keep out of reach of children

Directions

Other information

Inactive ingredients

acacia, carmine, carnauba wax, citric acid, corn starch, corn syrup, DL-alpha tocopherol, FD&C blue #1 aluminum lake, FD&C yellow #5 lake (tartrazine), FD&C yellow #6, FD&C yellow #6 aluminum lake, FD&C yellow #6 lake, flavors, hydrogenated coconut oil, hydrogenated vegetable oil, lecithin, medium chain triglycerides, methyl paraben, modified starch, phosphoric acid, pregelatinized modified starch, propyl paraben, propylene glycol, shellac, sodium benzoate, sorbic acid, sorbitol, sugar, titanium dioxide, water, white wax

Questions or comments?

1-800-986-0369 (Mon-Fri 9AM-5PM EST)

Alka Seltzer HB 90 ct

ALKA SELTZER 
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52642-226
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE750 mg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Colorpink, yellow, orangeScorescore with uneven pieces
ShapeROUNDSize70mm
FlavorSTRAWBERRY, LEMON, ORANGEImprint Code AS
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52642-226-9090 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/08/2013
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33102/08/2013
Labeler - BestCo Inc. (002149136)
Registrant - Bayer (112117283)
Establishment
NameAddressID/FEIBusiness Operations
BestCo Inc.002149136manufacture(52642-226)

Revised: 2/2016
Document Id: 2b95d0b8-a30b-667d-e054-00144ff8d46c
Set id: 2b95d0b8-a30a-667d-e054-00144ff8d46c
Version: 1
Effective Time: 20160212
 
BestCo Inc.