FDA label d3c29d36-dedb-6bf4-e053-2995a90ae773

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
9a00a65e-648a-f9aa-e053-2995a90a865b
SPL ID
d3c29d36-dedb-6bf4-e053-2995a90ae773
Version
3
Effective date
2021-12-22
Source export date
2026-10-12
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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:36:19

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. Ask a doctor before use if: taking a prescription drug or have a serious medical condition When using this product: Avoid contact with eyes or mucous membranes Do not use with other ointments, creams, or sprays Do not apply over large areas of the body or bandage Do not use with heating pad or device Stop use and ask a doctor if: conditions worsen, or if symptoms persist for more than seven (7) days, or clear up and reoccur. If pregnant or breast-feeding: Ask a healthcare professional before use. Keep out of reach of children: If accidentally swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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