FDA label 934614fc-0407-8ada-e053-2a95a90a0fc8

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
9345ebf7-703d-3bcb-e053-2995a90a4202
SPL ID
934614fc-0407-8ada-e053-2a95a90a0fc8
Version
1
Effective date
2019-09-24
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:31:15

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.

Reported adverse events (FAERS/openFDA)#

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