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NDC 21130-0171-75 Ultra Strength Antacid Relief Assorted fruit 1000 mg/1 Details

Ultra Strength Antacid Relief Assorted fruit 1000 mg/1

Ultra Strength Antacid Relief Assorted fruit is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by Safeway. 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: 21130-0171-75
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Product Information

NDC	21130-0171
Product ID	21130-171_79d5ff30-52a4-40d2-8ea8-0e238a912f36
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Ultra Strength Antacid Relief Assorted fruit
Proprietary Name Suffix	n/a
Non-Proprietary Name	Calcium Antacid
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, CHEWABLE
Route	ORAL
Active Ingredient Strength	1000
Active Ingredient Units	mg/1
Substance Name	CALCIUM CARBONATE
Labeler Name	Safeway
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	2023-12-31

Package

Package Images

NDC 21130-0171-75 (21130017175)

Pricing Information	N/A
NDC Package Code	21130-171-75
Billing NDC	21130017175
Package	160 TABLET, CHEWABLE in 1 BOTTLE (21130-171-75)
Marketing Start Date	2015-08-08
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL d71aa99d-8f1f-4079-b554-4ba270302506 Details

Active ingredient (in each tablet)

Calcium carbonate 1000 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 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 breast-feeding, ask a health professional before use.

Keep out of reach of children.

Directions

adults and children 12 years of age and over: chew 2-3 tablets as symptoms occur, or as directed by a doctor.

Other information

each tablet contains: elemental calcium 400 mg
do not use if printed seal under cap is torn or missing.
store at room temperature. keep the container tightly closed.

Inactive ingredients

adipic acid, corn starch, crospovidone, D&C red 27 lake, D&C red 30 lake, D&C yellow 10 lake, dextrose, FD&C blue 1 lake, FD&C yellow 6 lake, flavors, magnesium stearate, maltodextrin, sucrose, talc.

Principal Display Panel

COMPARE TO TUMS® Ultra strength active ingredient*

NDC 21130-171-68

Signature Care

Ultra Strength Antacid Relief Tablets

CAlCIUM CARBONATE 1000 mg

ASSORTED FRUIT FLAVOR

Chewable
Rich in calcium
Relief of:acid indigestion/heartburn

72 TABLETS

INGREDIENTS AND APPEARANCE

ULTRA STRENGTH ANTACID RELIEF ASSORTED FRUIT

calcium antacid tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21130-171
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D)	CALCIUM CARBONATE	1000 mg

Ingredient Name	Strength
Inactive Ingredients
ADIPIC ACID (UNII: 76A0JE0FKJ)
STARCH, CORN (UNII: O8232NY3SJ)
CROSPOVIDONE (UNII: 2S7830E561)
D&C RED NO. 27 (UNII: 2LRS185U6K)
D&C RED NO. 30 (UNII: 2S42T2808B)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SUCROSE (UNII: C151H8M554)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	orange, yellow, green, pink (reddish-pink)	Score	no score
Shape	ROUND	Size	17mm
Flavor	FRUIT (orange, cherry, lemon, lime)	Imprint Code	G171
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:21130-171-68	72 in 1 BOTTLE; Type 0: Not a Combination Product	08/08/2015
2	NDC:21130-171-75	160 in 1 BOTTLE; Type 0: Not a Combination Product	08/08/2015

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part331	08/08/2015

Labeler - Safeway (009137209)

Revised: 1/2022

Document Id: 79d5ff30-52a4-40d2-8ea8-0e238a912f36

Set id: d71aa99d-8f1f-4079-b554-4ba270302506

Version: 4

Effective Time: 20220112