FDA label c8ba7005-a8ee-417c-8015-be2a416cdc42

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
da2e00c8-b60b-4ff2-a5d1-5467d6ee2db4
SPL ID
c8ba7005-a8ee-417c-8015-be2a416cdc42
Version
1
Effective date
2020-02-17
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:23:37

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 • Avoid contact with the eyes and mucous membranes. Do ont use otherwise than as directed. Caution: Discontinue use if excessive irritation of the skin develops. When using this product Do not apply to wounds or damaged skin. Do not tightly bandage. Do not apply with external heat, such as electric heating pad, as this may result in excessive skin irritation or skin burn. Do not inhale. Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if • Hypersensitivity / allergy, rashes and or burning discomfort occur. • You experience pain, swelling or blistering. •Symptoms worsens •Symptoms persist for more than 7 days or clear up and occur again within a few days. If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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