FDA.reportPublic FDA data

FDA label 0cc44ebb-f70f-fa09-e063-6394a90a3fc9

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
0cc44014-b51e-f910-e063-6394a90a5060
SPL ID
0cc44ebb-f70f-fa09-e063-6394a90a3fc9
Version
1
Effective date
2023-12-18
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:36:46

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 - Allergy alert: This product contains natural rubber latex which may cause allergic reactions Do not use ■Skin ulcers, breakage, and infections ■Pregnant women ■People with allergies Stop use and ask a doctor if excessive irritation of the skin develops When using this product avoid contact with the eyes Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. This product is a daily health product and cannot replace drugs and medical devices.

Reported adverse events (FAERS/openFDA)#

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