Obagi Nu-Derm System Normal-Dry Skin Transformation Trial
- Product NDC
- 62032-913
- 11-digit product format
- 620320913
- Labeler code
- 62032
- Product ID
- 62032-913_f1292c32-db82-4875-b681-b984c56f9cff
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDE
- Dosage form
- KIT
- Labeler
- Obagi Cosmeceuticals LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-12-02
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Obagi Nu-Derm System Normal-Dry Skin Transformation Trial
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 197795 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62032-100-36 | Obagi Nu-Derm System Normal-Dry Skin Transformation Trial | 57 g in 1 BOTTLE, PLASTIC | CREAM | 28 g | 40 mg in 1g | 3 |
| 62032-101-36 | Obagi Nu-Derm System Normal-Dry Skin Transformation Trial | 57 g in 1 BOTTLE, PLASTIC | CREAM | 57 g | 40 mg in 1g | 3 |
| 62032-140-05 | Obagi Nu-Derm System Normal-Dry Skin Transformation Trial | 28 g in 1 TUBE | LOTION | 28 g | 50 mg in 1g | 3 |
| 62032-913-01 | Obagi Nu-Derm System Normal-Dry Skin Transformation Trial | 1 in 1 CARTON | KIT | 1 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 62032-100-36 | 62032010036 | 57 g in 1 BOTTLE, PLASTIC | 57 g | Historical |
| 62032-101-36 | 62032010136 | 57 g in 1 BOTTLE, PLASTIC | 57 g | Historical |
| 62032-140-05 | 62032014005 | 28 g in 1 TUBE | 28 g | Historical |
| 62032-913-01 | 62032091301 | 1 in 1 CARTON | | Historical |