FDA label ecd389e1-213e-24bc-e053-2a95a90ad556

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
6ce5f0d0-efbb-4a6a-a813-544586b16f72
SPL ID
ecd389e1-213e-24bc-e053-2a95a90ad556
Version
2
Effective date
2022-11-06
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:43:32

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 Because we utilize as many naturally derived ingredients as possible, our products may vary in color over time and with each new batch we make. These natural variations do not in any way affect the quality of efficacy of the product. █ For external use only. █ Ask a doctor before use if you have a condition that covers a large area of the body █ Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. █ Stop use and ask a doctor if the condition worsens or does not improve after regular use of this product as directed.

Reported adverse events (FAERS/openFDA)#

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