GOODSENSE ULTRA STRENGTH ANTACID PEPPERMINT - calcium carbonate tablet, chewable 
GoodSense

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.

----------

GOODSENSE Ultra Strength Antacid Peppermint Chewable Tablets

ACTIVE INGREDIENT (in each tablet)

Calcium carbonate 1000 mg

PURPOSE

Antacid

USE(S)

relieves:

WARNINGS

.

ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE

WHEN USING THIS PRODUCT

do not take more than 7 tablets in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.

IF PREGNANT OR/BREASTFEEDING,

ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

.

DIRECTIONS

OTHER INFORMATION

INACTIVE INGREDIENTS

corn starch, crospovidone, dextrose, flavor, magnesium stearate, maltodextrin, sucrose, talc.

PRINCIPAL DISPLAY PANEL

GOODSENSE
Ultra Strength

NDC 50804-176-68

Antacid
TABLETS

Calcium Carbonate 1000 mg

Fast Relief of


Peppermint Flavor
*Compare to active ingredient of Ultra Strength Tums®

72 Chewable Tablets



128
GOODSENSE ULTRA STRENGTH ANTACID PEPPERMINT 
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50804-176
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE1000 mg
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN (UNII: O8232NY3SJ)  
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
SUCROSE (UNII: C151H8M554)  
TALC (UNII: 7SEV7J4R1U)  
CROSPOVIDONE (UNII: 2S7830E561)  
Product Characteristics
ColorWHITEScoreno score
ShapeROUNDSize17mm
FlavorPEPPERMINTImprint Code G171
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50804-176-6872 in 1 BOTTLE; Type 0: Not a Combination Product08/08/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart33108/08/2018
Labeler - GoodSense (076059836)
Establishment
NameAddressID/FEIBusiness Operations
Guardian Drug Company119210276MANUFACTURE(50804-176)

Revised: 1/2022
Document Id: 8719d2a9-7634-4c24-a5c6-cb0dc97c7e70
Set id: 04950b56-7760-4b6c-8110-86b6a3f795b4
Version: 2
Effective Time: 20220113
 
GoodSense