FDA label 7571e1f3-981a-4141-ba71-261f4bed6fa2

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
382b5062-2fcb-4b30-b430-a020700813cb
SPL ID
7571e1f3-981a-4141-ba71-261f4bed6fa2
Version
2
Effective date
2012-12-20
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 05:51:34

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. Children under 2 years of age should be seen by a physician. Initial exacerbation of symptoms may occur. To avoid contamination, do not touch the tip of the container to any surface. Use within 30 days of opening. Expiration date only refers to unopened bottle. Replace cap tightly after every use. Contact wearers: consult physician prior to using. The use of this container by more than one person may spread infection. If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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