FDA label 6fd20196-011e-4834-adc0-6601f3ceb1e8

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
04c58bf9-acbf-4a3d-a084-0110af1cfa3d
SPL ID
6fd20196-011e-4834-adc0-6601f3ceb1e8
Version
3
Effective date
2025-06-13
Source export date
2026-10-12
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/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:44:41

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

Notice 1.This product is a disinfectant for external use. it is forbidden to take it orally and keep it out ofreach of children. 2.This product is flammable, keep away from fire sources. 3. infants and children should use it under adult supervision to prevent misuse and ingestion. 4. This product is irritating, avoid contact with eyes, and do not insert into ear canal. 5. lf skin redness, inflammation, swelling, pain persists or worsens, infection occurs, or use lasts formore than a week, please stop using it or consult a doctor6. This product is for one-time use, please do not reuse it.

Reported adverse events (FAERS/openFDA)#

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