FDA label 7f8e9255-7895-011f-e053-2a91aa0a6cac

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
4b338dc0-108a-3c18-e054-00144ff88e88
SPL ID
7f8e9255-7895-011f-e053-2a91aa0a6cac
Version
2
Effective date
2019-01-16
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:35:08

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

1. Do not use in the following cases(Eczema and scalp wounds) 2.Side Effects 1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor 3.General Precautions 1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately 2)This product is for exeternal use only. Do not use for internal use 4.Storage and handling precautions 1)If possible, avoid direct sunlight and store in cool and area of low humidity 2)In order to maintain the quality of the product and avoid misuse 3)Avoid placing the product near fire and store out in reach of children

Reported adverse events (FAERS/openFDA)#

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