Antacid Tablet, Chewable
FDA Label NDC 54738-030

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Richmond Pharmaceuticals, Inc. for the product Antacid (NDC 54738-030). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, keep out of reach of children., directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Active Ingredient

→ Purpose

→ Uses

→ Warnings

→ Keep Out Of Reach Of Children.

→ Directions

→ Other Information

→ Inactive Ingredients

→ Questions Or Comments

→ Package Label.principal Display Panel

Active Ingredient

(in each tablet)

Calcium Carbonate 500 mg

Purpose

Antacid

Uses

relieves

acid indigestion
heartburn
sour stomach

Warnings

Ask a doctor before use if you have

kidney stones
a calcium-restricted diet
ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs.
Stop use and ask a doctor if symptoms last more than 2 weeks.

Keep Out Of Reach Of Children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

chew 1-2 tablets as symptoms occurs.
do not take more than 8 tablets in 24 hours
do not use the maximum dosage for more than 2 weeks

Other Information

each tablet contains: calcium 200 mg
store at room temperature 15-30 °C (59-86 °F)

Inactive Ingredients

Al-lakes (D&C red #27, D&C yellow # 10, FD&C blue #1, FD&C yellow # 6), dextrose, flavors (cherry, lemon, lime, orange), magnesium stearate, maltodextrin