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NDC 69790-0089-33 Uline Antacid 420 mg/1 Details

Uline Antacid 420 mg/1

Uline Antacid is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by Uline. 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: 69790-0089-33
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Product Information

NDC	69790-0089
Product ID	69790-089_debc3184-6bb1-11d1-e053-2995a90af277
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	Uline 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	420
Active Ingredient Units	mg/1
Substance Name	CALCIUM CARBONATE
Labeler Name	Uline
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 69790-0089-33 (69790008933)

Pricing Information	N/A
NDC Package Code	69790-089-33
Billing NDC	69790008933
Package	50 PACKET in 1 BOX (69790-089-33) / 2 TABLET, CHEWABLE in 1 PACKET
Marketing Start Date	2019-10-07
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 9014f295-e816-9bcd-e053-2a95a90ae103 Details

SPL UNCLASSIFIED SECTION

Drug Facts

SPL UNCLASSIFIED SECTION

Active ingredients (in each tablet)

Calcium Carbonate 420 mg

SPL UNCLASSIFIED SECTION

Purpose

Antacid

SPL UNCLASSIFIED SECTION

Uses

relieves

acid indigestion
sour stomach
heartburn
upset stomach associated with these symptoms

SPL UNCLASSIFIED SECTION

Warnings

SPL UNCLASSIFIED SECTION

Do not use

the maximum dosage of this product for more than 2 weeks except under the advice and supervision of a

physician or take more than 19 tablets in a 24 hour period.

SPL UNCLASSIFIED SECTION

Ask a doctor or pharmacist before use if you

are presently taking a prescription drug. Antacids may interact with certain prescription drugs.
have kidney disease

SPL UNCLASSIFIED SECTION

When using this product

do not use more than 19 tablets in a 24 hour period. If symptoms persist for more than 2 weeks. stop using this product and see a doctor.

SPL UNCLASSIFIED SECTION

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

SPL UNCLASSIFIED SECTION

Keep out of the reach of children.

SPL UNCLASSIFIED SECTION

Directions

Adults and children: (12 years and older) Chew 2 tablets every 2 - 3 hours as symptoms occur, repeat hourly if needed. Do not exceed 19 tablets in 24 hours.

Children under 12 years: Ask a doctor

SPL UNCLASSIFIED SECTION

Other information

calcium content per tablet: 168 mg
phenylketonurics: each tablet may contain 1.5 mg phenylalanine
store at room temperature 59-86°F (15-30°C) in a dry place
tamper-evident sealed packets
do not use any opened or torn packets

SPL UNCLASSIFIED SECTION

Inactive ingredients

aspartame*, croscarmellose sodium*, gum acacia*, magnesium stearate, maltodextrin, mineral oil*, mint flavor, sorbitol*, sucrose*

* may contain

SPL UNCLASSIFIED SECTION

Questions or comments? 1-800-295-5510

PRINCIPAL DISPLAY PANEL

ULINE

ANTACID

Tamper evident sealed packets:

Do not use if packet is open or torn.

Pull to Open

Calcium Carbonate 420 mg

• Do not swallow tablets whole

50 Packets

2 Tablets Each

PRINCIPAL DISPLAY PANEL

ULINE

ANTACID

Tamper evident sealed packets:

Do not use if packet is open or torn.

Pull to Open

Calcium Carbonate 420 mg

• Do not swallow tablets whole

50 Packets

2 Tablets Each

INGREDIENTS AND APPEARANCE

ULINE ANTACID

calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69790-089
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	420 mg

Ingredient Name	Strength
Inactive Ingredients
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MAGNESIUM STEARATE (UNII: 70097M6I30)
SUCROSE (UNII: C151H8M554)
ACACIA (UNII: 5C5403N26O)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	12mm
Flavor	MINT	Imprint Code	FR;8
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:69790-089-33	50 in 1 BOX	10/07/2019
1		2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part331	10/07/2019

ULINE ANTACID

calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69790-820
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	420 mg

Ingredient Name	Strength
Inactive Ingredients
ASPARTAME (UNII: Z0H242BBR1)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
SORBITOL (UNII: 506T60A25R)
MINERAL OIL (UNII: T5L8T28FGP)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	11mm
Flavor		Imprint Code	AZ;036
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:69790-820-33	50 in 1 BOX	10/07/2019
1		2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part331	10/07/2019

Labeler - Uline (039612668)

Registrant - Unifirst First Aid Corporation (832947092)

Name	Address	ID/FEI	Business Operations
Establishment
Prestige Packaging		080667761	pack(69790-089, 69790-820)

Name	Address	ID/FEI	Business Operations
Establishment
Medique Products		086911794	pack(69790-820, 69790-089)

Revised: 5/2022

Document Id: debc3184-6bb1-11d1-e053-2995a90af277

Set id: 9014f295-e816-9bcd-e053-2a95a90ae103

Version: 6

Effective Time: 20220511

Search by Drug Name or NDC

NDC 69790-0089-33 Uline Antacid 420 mg/1 Details

Uline Antacid 420 mg/1

MedlinePlus Drug Summary

Product Information

Package

Package Images

NDC 69790-0089-33 (69790008933)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 9014f295-e816-9bcd-e053-2a95a90ae103 Details

SPL UNCLASSIFIED SECTION

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PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

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