FDA label 574ffbd2-b53e-472f-804d-7a143da445e8

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
9f73cae2-7bfe-43fc-aaf0-b06cdb51f51b
SPL ID
574ffbd2-b53e-472f-804d-7a143da445e8
Version
2
Effective date
2020-01-02
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:52:23

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: Do not swallow. Do not use if allergic to Asteracea (daisy) family of flowers. Do not use for yeast infections (may be used in conjuction with yeast medication). Use only as directed. For external use only. Brief tingling may occur. If conditions worsens or does not improve, contact a health care professional. Avoid contact with eyes. WE SUGGEST THAT YOU NOT USE ALCOHOL DURING AN OUTBREAK OR WHEN USING THIS PRODUCT.

Reported adverse events (FAERS/openFDA)#

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