FDA label d05cbc99-3dc2-4db5-9b86-6e8ef41f533d

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
a27badf6-ce29-4aa1-aab7-01cd2c106c92
SPL ID
d05cbc99-3dc2-4db5-9b86-6e8ef41f533d
Version
2
Effective date
2015-05-04
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:23:04

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS When using this product there are no known drug interactions Keep out of reach of children. Directions ■ Adults: chew thoroughly and swallow one or two tablets as needed after meals or at bedtime ■ do not exceed 6 tablets in 24 hours ■ do not increase dosage unless recommended by your doctor. Other information ■ store at room temperature 59°- 86°F (15°-30°C) ■ protect from excessive moisture ■ do not use if foil backing is torn ■ Calcium content per tablet: 98 mg Inactive ingredients D&C red #30, calcium phosphate, magnesium stearate, silicon dioxide, sorbitol, sucrose

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.