FDA label 0fe6a5d3-1541-4a87-8289-7f24907aa588

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
6534136f-6f6e-4bcc-9cb5-d70eb24f1e23
SPL ID
0fe6a5d3-1541-4a87-8289-7f24907aa588
Version
1
Effective date
2012-07-06
Source export date
2026-10-12
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:22:10

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Ask a doctor before you use if you have • kidney disease • a magnesium or potassium-restricted diet • abdominal pain, nausea, or vomiting • noticed a sudden change in bowel habits that persists over a period of 2 weeks • already used a laxative for a period longer than 1 week Ask a doctor or pharmacist before use if your are taking any other drug. Take this product 2 or more hours before or after other drugs. Laxatives may affect how other drugs work. Stop use and ask a doctor if you have rectal bleeding or failure to have a bowel movement after use. These could be signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Adverse reactions cross-check#

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Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

Distributed by: Vi-Jon One Swan Drive Smyrna, TN 37167 Additional barcode labeling by: Physicians Total Care, Inc. Tulsa, Oklahoma 74146

Reported adverse events (FAERS/openFDA)#

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