FDA label 0d762cea-b5e1-6ff1-e063-6394a90aee03

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
f88829f2-d900-4b78-b2cc-eebd76c326cd
SPL ID
0d762cea-b5e1-6ff1-e063-6394a90aee03
Version
4
Effective date
2023-12-26
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:05:48

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 (For external use only) Do not use this product if Pregnant or breast-feeding, ask a health professional before use. In case of accidental overdose, contact a doctor or Poison Control Center immediately. Tamper Evident "Warranty Void...Seal...label atop the container is broken." When using this product Do not exceed the recommended daily dosage unless directed by a doctor. Certain persons can develop allergic reactions to ingredients in this product. Do not put this product into the rectum by using fingers or any medical device or applicator. Stop use and ask a doctor if The symptom being treated does not subside or if redness, irritation, swellinh, pain, or other symptoms develop or increase. Keep out of reach of children In case of accidental ingestion, seek medical attention immediately.

Reported adverse events (FAERS/openFDA)#

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