Active Ingredients
Calcium Carbonate 420 mg
The following Structured Product Label (SPL) was submitted to the FDA by Uline for the product Uline Antacid (NDC 69790-089). 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 ingredients, purpose, uses, do not use, ask a doctor or pharmacist before use if you are, stop use and ask a doctor if, if pregnant or breast feeding,, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Calcium Carbonate 420 mg
Antacid
For the relief of the following symptoms
physician or take more than 19 tablets in a 24 hour period.
ask a health professional before use.
Adults and children: (12 years and older) Chew 2 tablets every 2 or 3 hours as symptoms occur or as directed by a physician. Do notexceed 19 tablets in 24 hours.
Children under 12 years: Do not give to children under 12 years of age.
aspartame*, croscarmellose sodium*, gum acacia*, magnesium stearate, maltodextrin, mineral oil*, mint flavor, sorbitol*, sucrose*
* may contain
1-800-295-5510
ULINE
Tamper evident sealed packets:
Do not use if packet is open or torn.
ANTACID
Pull to Open
Calcium Carbonate 420 mg
• Chew or crush tablets completely before swallowing
• Do not swallow tablets whole
50 Packets
2 Tablets Each
ULINE
Tamper evident sealed packets:
Do not use if packet is open or torn.
ANTACID
Pull to Open
Calcium Carbonate 420 mg
• Chew or crush tablets completely before swallowing
• Do not swallow tablets whole
50 Packets
2 Tablets Each
* Please review the disclaimer below.