Obagi Medical - Nu-Derm System - Normal to Dry - Skin Transformation Kit
- Product NDC
- 62032-526
- 11-digit product format
- 620320526
- Labeler code
- 62032
- Product ID
- 62032-526_935a1c17-63d7-43ba-b02c-0736c0ca1277
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE, ZINC OXIDE
- Dosage form
- KIT
- Labeler
- OMP, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-12-10
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62032-526-06 | Obagi Medical - Nu-Derm System - Normal to Dry - Skin Transformation Kit | 1 in 1 CARTON | KIT | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62032-526 | OBAGI MEDICAL - NU-DERM SYSTEM - NORMAL TO DRY - SKIN TRANSFORMATION KIT (OCTINOXATE, ZINC OXIDE) KIT [OMP, INC.] | 1 | Legacy NDC, 1 package rows | 20151211_935a1c17-63d7-43ba-b02c-0736c0ca1277.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 62032-526-06 | 62032052606 | 1 in 1 CARTON | Historical |