Obagi-C Rx system C-Therapy Night Skin Lightening with Vitamins C and E
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
- Brand name
- Obagi-C Rx system C-Therapy Night Skin Lightening with Vitamins C and E
- Generic name
- HYDROQUINONE
- Manufacturer
- Obagi Cosmeceuticals LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 81e2e734-01fe-4568-903a-92993bf40887
- SPL ID
- 2e9d9417-8b73-4d00-9783-c0d14f1a9cbc
- Version
- 7
- Effective date
- 2020-06-01
- Source export date
- 2026-09-28
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:01
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Obagi-C Rx system C-Therapy Night Skin Lightening with Vitamins C and E | openfda.brand_name | |
| generic name | HYDROQUINONE | openfda.generic_name | |
| manufacturer name | Obagi Cosmeceuticals LLC | openfda.manufacturer_name | |
| ndc | package | 62032-105-36 | openfda.package_ndc |
| ndc | product | 62032-105 | openfda.product_ndc |
| ndc11 | package | 62032010536 | derived:openfda.package_ndc |
| rxcui | 197795 | openfda.rxcui | |
| spl id | 2e9d9417-8b73-4d00-9783-c0d14f1a9cbc | id | |
| spl set id | 81e2e734-01fe-4568-903a-92993bf40887 | set_id | |
| unii | XV74C1N1AE | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS • Hydroquinone is a skin-bleaching agent, which may produce unwanted cosmetic effects if not used as directed. The physician should be familiar with the contents of this insert before prescribing or dispensing this product. • Test for skin sensitivity before using by applying a small amount to an unbroken patch of skin and check within 24 hours. Minor redness is not a contraindication, but where there is itching or vesicle formation or excessive inflammatory response, the product should be discontinued and a physician consulted. Close patient supervision is recommended. • Avoid contact with eyes, nose, mouth, and lips. In case of accidental contact, the patient should rinse thoroughly with water and contact a physician. • Sunscreen use is an essential aspect of hydroquinone therapy because even minimal sunlight exposure sustains melanocytic activity. The Obagi-C ® Rx System C-Therapy Night Cream contains sodium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. The overall prevalence of sulfite sensitivity in the general population is unknown and probably low. Sulfite sensitivity is seen more frequently in asthmatic than in nonasthmatic people.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS No systemic adverse reactions have been reported. Occasional hypersensitivity (localized contact dermatitis) may occur, in which case the product should be discontinued and physician notified immediately. To report SUSPECTED ADVERSE REACTIONS, contact Obagi Medical Products, a division of Valeant Pharmaceuticals North America LLC, at 1-800-321-4576 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.