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NDC 49348-0055-39 SUNMARK Calcium Antacid 750 mg/1 Details

SUNMARK Calcium Antacid 750 mg/1

SUNMARK Calcium Antacid is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by Strategic Sourcing Services LLC. The primary component is CALCIUM CARBONATE.

MedlinePlus Drug Summary

Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 49348-0055-39
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Product Information

NDC	49348-0055
Product ID	49348-055_63f9d734-98d4-46d0-82f5-2259521acb67
Associated GPIs	48300010000520
GCN Sequence Number	002690
GCN Sequence Number Description	calcium carbonate TAB CHEW 300MG(750) ORAL
HIC3	D4B
HIC3 Description	ANTACIDS
GCN	07894
HICL Sequence Number	001163
HICL Sequence Number Description	CALCIUM CARBONATE
Brand/Generic	Generic
Proprietary Name	SUNMARK Calcium Antacid
Proprietary Name Suffix	n/a
Non-Proprietary Name	Calcium carbonate
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, CHEWABLE
Route	ORAL
Active Ingredient Strength	750
Active Ingredient Units	mg/1
Substance Name	CALCIUM CARBONATE
Labeler Name	Strategic Sourcing Services LLC
Pharmaceutical Class	Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part331
Listing Certified Through	2024-12-31

Package

Package Images

NDC 49348-0055-39 (49348005539)

Pricing Information
NDC Package Code	49348-055-39
Billing NDC	49348005539
Package	80 TABLET, CHEWABLE in 1 BOTTLE (49348-055-39)
Marketing Start Date	2019-09-24
NDC Exclude Flag	N
Price Per Unit	0.02774
Pricing Unit	EA
Effective Date	2024-02-21
NDC Description	SM CAL ANTACID 750 MG CHEW TAB
Pharmacy Type Indicator	C/I
OTC	Y
Explanation Code	1
Classification for Rate Setting	G
As of Date	2024-02-21

This pricing file, entitled the NADAC (National Average Drug Acquisition Cost) files, provide state Medicaid agencies with covered outpatient drug prices by averaging survey invoice prices from retail community pharmacies across the United States. These pharmacies include independent retail community pharmacies and chain pharmacies. The prices are updated on a weekly and monthly basis

Standard Product Labeling (SPL)/Prescribing Information SPL 5cbc3239-d87d-4f86-a63a-1b5b4e4ea490 Details

Active ingredient (in each tablet)

Calcium carbonate 750 mg

Purpose

Antacid

SPL UNCLASSIFIED SECTION

Uses

relieves:

acid indigestion
heartburn

Warnings

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

do not take more than 10 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.

keep out of reach of children.

Directions

chew 2-4 tablets as symptoms occur, or as directed by a doctor

Other information

store at room temperature.
Phenylketonurics: contains phenylalanine, less than 1 mg per tablet

Inactive ingredients

adipic acid, aspartame, FD&C yellow 6 aluminum lake, flavor, magnesium stearate, maltodextrin, microcrystalline cellulose, sorbitol

PDP

sunmark

COMPARE TO THE ACTIVE INGREDIENT IN TUMS® E-X SUGAR FREE*

NDC 49348-055-39

sugar free

antacid tablets

Extra strength

calcium carbonate 750 mg

Fast relief of heartburn & acid indigestion

Natural and Artificial Flavor

ORANGE FLAVOR

80 Chewable Tablets

INGREDIENTS AND APPEARANCE

SUNMARK CALCIUM ANTACID

calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49348-055
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CATION	750 mg

Ingredient Name	Strength
Inactive Ingredients
ADIPIC ACID (UNII: 76A0JE0FKJ)
ASPARTAME (UNII: Z0H242BBR1)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SORBITOL (UNII: 506T60A25R)

Product Characteristics
Color	orange	Score	no score
Shape	ROUND	Size	16mm
Flavor	ORANGE	Imprint Code	G174
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:49348-055-39	80 in 1 BOTTLE; Type 0: Not a Combination Product	09/24/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part331	09/24/2019

Labeler - Strategic Sourcing Services LLC (116956644)

Revised: 1/2022

Document Id: 63f9d734-98d4-46d0-82f5-2259521acb67

Set id: 5cbc3239-d87d-4f86-a63a-1b5b4e4ea490

Version: 6

Effective Time: 20220106