FDA label f6353130-207b-5db6-e053-2a95a90a34c4

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
f6353130-207a-5db6-e053-2a95a90a34c4
SPL ID
f6353130-207b-5db6-e053-2a95a90a34c4
Version
1
Effective date
2023-03-06
Source export date
2026-11-06
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/bbdc0a42bf44145a63c3752991067bece7e2a518be6cc14943d33c4987faa012/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:13:07

Warnings cross-check#

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

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warning 1. This product is a health care product and does not replace drugs and medical devices for treatment 2. Keep warm after use, and do not catch cold by the wind 3. This product is for external use, please do not swallow it 4. If it gets into your eyes, please wash it with clean water immediately 5. In case of discomfort, rash and other conditions during or after the use of this product, immediately stop using and seek medical advice 6. Do not use it when the skin of the use site is ulcerated or damaged 7. Please place this product in a place that is not easy for children to touch

warnings and cautions

People with a history of myocardial infarction, cerebral infarction, and stroke should be cautious; During menstruation, patients with intracerebral hemorrhage, severe hypertension, the elderly, pregnancy, lactation, infants and allergic constitution are prohibited. Patients with non-serious hypertension should use it under stable blood pressure

Reported adverse events (FAERS/openFDA)#

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