Uline Antacid: Package Insert and Label Information

ULINE ANTACID- calcium carbonate tablet, chewable
Uline

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.

Drug Facts

Active ingredients (in each tablet)

Calcium Carbonate 420 mg

Purpose

Antacid

Uses

relieves

• acid indigestion
• sour stomach
• heartburn
• upset stomach associated with these symptoms

Warnings

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.

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

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.

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

Keep out of the reach of children.

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

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

Inactive ingredients

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

* may contain

Questions or comments? 1-800-295-5510

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

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

ULINE ANTACID calcium carbonate tablet, chewable

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69790-089 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (CALCIUM CATION and CARBONATE ION) CALCIUM CARBONATE 420 mg

Inactive Ingredients Ingredient Name Strength MALTODEXTRIN MAGNESIUM STEARATE SUCROSE ACACIA

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

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:69790-089-33 50 PACKET in 1 BOX contains a PACKET 1 2 TABLET, CHEWABLE in 1 PACKET This package is contained within the BOX (69790-089-33)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date 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 DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (CALCIUM CATION and CARBONATE ION) CALCIUM CARBONATE 420 mg

Inactive Ingredients Ingredient Name Strength ASPARTAME MAGNESIUM STEARATE MALTODEXTRIN CROSCARMELLOSE SODIUM (CROSCARMELLOSE) SORBITOL MINERAL OIL

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

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:69790-820-33 50 PACKET in 1 BOX contains a PACKET 1 2 TABLET, CHEWABLE in 1 PACKET This package is contained within the BOX (69790-820-33)

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

Labeler — Uline (039612668)

Registrant — Unifirst First Aid Corporation (832947092)

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

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

Revised: 05/2022 Uline