Other
Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Uline for the product Uline Antacid (NDC 69790-820). 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 other, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - ask doctor/pharmacist, otc - when using, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Active ingredient (in each tablet)
Calcium Carbonate 420 mg
Purpose
Antacid
Uses
relieves
Warnings
Do not use
doctor
Ask a doctor or pharmacist before use if you
When using this product
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
Inactive ingredients
aspartame, croscarmellose sodium, magnesium stearate, maltodextrin, mint flavor, sorbitol
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.
ANTACID
Pull to Open
Calcium Carbonate 420 mg
• Do not swallow tablets whole
50 Packets
2 Tablets Each
* Please review the disclaimer below.