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 rev 4-13-21
(click image for full-size original)

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 2
(click image for full-size original)
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

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