DETOX DROPS ACNE TONER

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)

Brand name
DETOX DROPS ACNE TONER
Generic name
ACNE TONER
Manufacturer
KENDO HOLDINGS INC.
Product type
HUMAN OTC DRUG
SPL set ID
35bcdb22-550e-b27c-e063-6294a90a2e5b
SPL ID
4008e932-d9d0-845d-e063-6294a90a6d07
Version
3
Effective date
2025-09-30
Source export date
2026-11-06
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/8ec9b1418c25a8bb472a36e6bc0b2cbabb210d48d5dd734197e022d21529ed58/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run
20261106T075659Z
Imported at
2026-11-06 09:15:59
Harmonized routes table
Harmonized routes
TOPICAL

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 FOR EXTERNAL USE ONLY WHEN USING THIS PRODUCT SKIN IRRITATION AND DRYNESS IS MORE LIKELY TO OCCUR IF YOU USE ANOTHER TOPICAL ACNE MEDICATION AT THE SAME TIME. iF IRRITATION OCCURS, ONLY USE ONE TOPICAL ACNE MEDICATION AT A TIME AVOID CONTACT WITH EYES. IF EYE CONTACT OCCURS, FLUSH THOROUGHLY WITH WATER.

Reported adverse events (FAERS/openFDA)#

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