Obagi Nu-Derm Fx System Normal-Oily Skin Transformation Complexion Brightening System

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
Obagi Nu-Derm Fx System Normal-Oily Skin Transformation Complexion Brightening System
Generic name
HOMOSALATE, OCTISALATE, ZINC OXIDE
Manufacturer
Obagi Cosmeceuticals LLC
Product type
HUMAN OTC DRUG
SPL set ID
49cd9e72-4e25-4ff9-aefc-467733b105be
SPL ID
113b4fa4-e6de-42f5-aa22-518aa22c774a
Version
4
Effective date
2025-10-23
Source export date
2026-10-27
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/2026-10-27/35717de05250cd386420cc8ede3b6010b48d18eea2af59afb0617fcabca634ec/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:05:32

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 Do not use on damaged or broken skin Stop use and ask a doctor if rash occurs When using this product keep out of eyes. Rinse with water to remove. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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