FDA label 500846e1-190d-91fb-e063-6394a90a157f

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
50044b55-854f-ca52-e063-6394a90a0e54
SPL ID
500846e1-190d-91fb-e063-6394a90a157f
Version
2
Effective date
2026-04-22
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:15:25

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

For external use only."Do not use if seal under cap is broken or missing."Close the lid tightly after use.Do not use this product if you are allergic to any of its ingredients.Do not use on children under 2 years of age unless directed by a doctor. Ask a doctor before use if you have Diabetes.When using this productAvoid contact with the eyes. Stop use and ask a doctor if- Irritation occurs There is no improvement within 4 weeks.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.