NDC 62032-142 - Obagi-C Fx System Normal-Oily Skin Brightening System With Arbutin
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 62032-142
- Package NDCs from labels
- 62032-142-11
- Manufacturer
- Obagi Cosmeceuticals LLC | Universal Packaging Systems, Inc. DBA: PakLab | Swiss American CDMO, LLC | Bay Cities Container Corporation
- Effective date
- 2019-10-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| OBAGI-C ® FX SYSTEM NORMAL-OILY SKIN BRIGHTENING SYSTEM WITH ARBUTIN | Obagi Cosmeceuticals LLC | Universal Packaging Systems, Inc. DBA: PakLab | Swiss American CDMO, LLC | Bay Cities Container Corporation | 2019-10-29 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62032-142-11 | Obagi-C Fx System Normal-Oily Skin Brightening System With Arbutin | 85 g in 1 TUBE | LOTION | 85 g | 50 mg in 1g | 1 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| MD Mineral BB Creme Broad Spectrum SPF 50 Water Resistant (80min) Mineral Sunscreen LIGHT | TITANIUM DIOXIDE AND ZINC OXIDE | MDSolarSciences | a7f906f6-3041-4c24-955d-90cdd402dd02 | 2025-11-03 | Warnings | SOI2LOH54Z |
| Com-Pare2 Dual Yeast Relief Plus Multi-symptom Formula | CANDIDA ALBICANS, WOOD CREOSOTE, SODIUM CHLORIDE, SULPHUR | TRP Company | 42b6b9b9-a673-0bba-e063-6394a90a8866 | 2025-11-03 | Warnings | 451W47IQ8X |
| Calamine Plus Pramoxine HCl | CALAMINE PLUS NO TOUCH SPRAY | Premier Brands of America Inc. | 36481d67-2346-470b-e063-6294a90aae99 | 2025-11-03 | Warnings | SOI2LOH54Z |
| Biopo Facial Mineral Sunscreen-Non Tinted SPF 40 | BIOPO FACIAL MINERAL SUNSCREEN-NON TINTED SPF 40 | Guangzhou Ariel Biotech Co., Ltd. | 42bc865f-29bd-da90-e063-6294a90aa16d | 2025-11-03 | Warnings | SOI2LOH54Z |
| Biopo Facial Mineral Sunscreen- Tinted SPF 40 | BIOPO FACIAL MINERAL SUNSCREEN- TINTED SPF 40 | Guangzhou Ariel Biotech Co., Ltd. | 42bd8bce-2959-266a-e063-6394a90a9a41 | 2025-11-03 | Warnings | SOI2LOH54Z |
| Systane Complete PF | PROPYLENE GLYCOL EMULSION | Alcon Laboratories, Inc. | 798ffdde-1dba-4a3f-a0b6-937f9e958cca | 2025-11-03 | Warnings | 6DC9Q167V3 |
| Potassium Chloride in Dextrose and Sodium Chloride | DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, AND POTASSIUM CHLORIDE | ICU Medical Inc. | d8ee14e9-6733-4813-9f21-2b043a5f7188 | 2025-11-02 | Warnings, Adverse reactions | 451W47IQ8X |
| GoodSense SPF 30 Sunscreen | AVOBENZONE 3%, HOMOSALATE 10%, OCTISALATE 5%, OCTOCRYLENE 10% | Geiss, Destin, & Dunn, Inc. | c23c754a-9441-0a05-e053-2995a90afc55 | 2025-11-02 | Warnings | V06SV4M95S 4X49Y0596W |
| SPF 30 Sport Sunscreen GoodSense | AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 8% | Geiss, Destin, & Dunn, Inc | a22c6359-435d-626b-e053-2a95a90ae0c6 | 2025-11-02 | Warnings | V06SV4M95S 4X49Y0596W |
| Dextrose and Sodium Chloride | DEXTROSE MONOHYDRATE AND SODIUM CHLORIDE | ICU Medical Inc. | 4555b1bf-6d97-4798-a63d-6d34291c85ce | 2025-11-02 | Warnings, Adverse reactions | 451W47IQ8X |
| Sterile Water | WATER | ICU Medical Inc. | aab10f03-26ae-4dbc-a481-ef025e48b405 | 2025-11-02 | Warnings, Adverse reactions | 059QF0KO0R |
| Potassium Chloride in Sodium Chloride | SODIUM CHLORIDE AND POTASSIUM CHLORIDE | ICU Medical Inc. | 9dd1c001-73b3-41d4-9a96-61f6ad3a5dc3 | 2025-11-02 | Warnings, Adverse reactions | 451W47IQ8X |
| Sterile Water | WATER | ICU Medical Inc. | e3484bc6-ed7f-43ef-9d49-c131a8dff2dd | 2025-11-02 | Warnings, Adverse reactions | 059QF0KO0R |
| Sodium Chloride | SODIUM CHLORIDE | ICU Medical Inc. | 3cfdeee0-ff14-4341-8396-b11c2a037c60 | 2025-11-02 | Warnings, Adverse reactions | 451W47IQ8X |
| Potassium Chloride in Sodium Chloride | SODIUM CHLORIDE AND POTASSIUM CHLORIDE | ICU Medical Inc. | 243fe8fc-996a-4855-8daf-069628e547c4 | 2025-11-02 | Warnings, Adverse reactions | 451W47IQ8X |
| Lactated Ringers and Dextrose | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, AND DEXTROSE MONOHYDRATE | ICU Medical Inc. | d310d170-5eeb-471b-af1a-0e845001d21d | 2025-11-02 | Warnings, Adverse reactions | 451W47IQ8X |
| ProCure ClamaPlex | ZINC OXIDE 20.625, MENTHOL 0.44, WHITE PETROLATUM 66.335 | Twin Med LLC | 3d366857-5178-9032-e063-6294a90a40f3 | 2025-11-01 | Warnings | SOI2LOH54Z |
| MyHealth Alcohol Antiseptic Hand Sanitizer | ALCOHOL | Aeroflex Industria de Aerosol Ltda | f8eeb819-ec48-41a4-920c-7cdae55d7ecd | 2025-10-31 | Warnings | 3K9958V90M |
| MyHealth Advanced Hand Sanitizer | ALCOHOL | Aeroflex Industria de Aerosol Ltda | 0e3b2c36-57d7-438b-a2fc-fa9f00d9a552 | 2025-10-31 | Warnings | 3K9958V90M |
| Wet Ones Antibacterial Hand Wipes - Eucalyptus and Mint | BENZALKONIUM CHLORIDE | Edgewell Personal Care Brands LLC | efb832d3-cc63-4d58-e053-2a95a90a642b | 2025-10-31 | Warnings | F5UM2KM3W7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.