FDA.reportPublic FDA data

FDA label 9345385d-2c7e-5ce8-e053-2995a90aba42

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
92c9f5c2-0d82-f769-e053-2a95a90a1170
SPL ID
9345385d-2c7e-5ce8-e053-2995a90aba42
Version
2
Effective date
2019-09-24
Source export date
2026-08-01
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/0689a4374f1490600b5244071db3b04bd3bbc29ceda7a856edb8225323adf20a/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:00:14

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

If skin shows the following reactions while using 3G AB_Solution, reduce the amount of use drastically or discontinue use. 1. If itching continues for 7-10 days 2. If skin experiences a burning sensation or becomes reddish (dry skin type, particularly extremely dry skin) 3. If dead skin cells are generated drastically * If you are receiving skin treatment due to skin diseases consult your doctor before use.