Obagi-C C-Rx System Normal-Dry Skin Intervention

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-C C-Rx System Normal-Dry Skin Intervention
Generic name: HYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDE
Manufacturer: Obagi Cosmeceuticals LLC
Product type: HUMAN OTC DRUG
SPL set ID: ca931d1c-4df4-47ce-8d5c-cd8c3e38c02b
SPL ID: 8562c1e2-2e0a-4aba-911a-dd89f1c59b4a
Version: 3
Effective date: 2026-01-26
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:13:13

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Obagi-C C-Rx System Normal-Dry Skin Intervention	openfda.brand_name
generic name		HYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDE	openfda.generic_name
manufacturer name		Obagi Cosmeceuticals LLC	openfda.manufacturer_name
ndc	package	62032-916-01	openfda.package_ndc
ndc	package	62032-105-36	openfda.package_ndc
ndc	package	62032-140-09	openfda.package_ndc
ndc	package	62032-106-10	openfda.package_ndc
ndc	product	62032-916	openfda.product_ndc
ndc11	package	62032014009	derived:openfda.package_ndc
ndc11	package	62032010536	derived:openfda.package_ndc
ndc11	package	62032010610	derived:openfda.package_ndc
ndc11	package	62032091601	derived:openfda.package_ndc
rxcui		197795	openfda.rxcui
spl id		8562c1e2-2e0a-4aba-911a-dd89f1c59b4a	id
spl set id		ca931d1c-4df4-47ce-8d5c-cd8c3e38c02b	set_id

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.