Over-the-counter drug · UNAPPROVED DRUG OTHER
Obagi Nu-Derm System Normal-Oily Skin Transformation NDC 62032-919
hydroquinone, titanium dioxide, zinc oxide · Kit · Obagi Cosmeceuticals LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 62032-919-01 | 6203209190162032091901 | 1 KIT in 1 BAG (62032-919-01) * 1 TUBE in 1 CARTON (62032-811-09) / 85 g in 1 TUBE * 198 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-100-36) * 48 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-101-36)Marketed from Jun 25, 2025 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Obagi Nu-Derm System Normal-Oily Skin Transformation
- Generic name (nonproprietary)
- hydroquinone, titanium dioxide, zinc oxide
- Dosage form
- Kit
- Labeler
- Obagi Cosmeceuticals LLCNDC labeler code 62032
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Identifiers
- Product ID 62032-919_41157f8f-7840-42f7-85cd-f16fff7862ccSPL ID 41157f8f-7840-42f7-85cd-f16fff7862ccSPL set ID ef3ddd1e-9305-42bb-a5f8-559e8e641d83RxCUI 197795
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.
- NDC on a medical claim
N462032091901followed by a unit qualifier and the quantityPackage 62032-0919-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Uses helps prevent sunburn If used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun
Excerpt only. Read the full label for complete information.
About NDC 62032-919
- What is NDC 62032-919?
- 62032-919 is the product NDC for Obagi Nu-Derm System Normal-Oily Skin Transformation kit, listed with the FDA by Obagi Cosmeceuticals LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Obagi Nu-Derm System Normal-Oily Skin Transformation (Hydroquinone, Titanium dioxide, Zinc oxide).
- Who is the labeler?
- Obagi Cosmeceuticals LLC, NDC labeler code 62032. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Obagi Nu-Derm System Normal-Oily Skin Transformation?
- 1 other product NDC are listed under this name. See all Obagi Nu-Derm System Normal-Oily Skin Transformation NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Obagi Nu-Derm System Normal-Oily Skin Transformation products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Obagi Nu-Derm System Normal-Oily Skin Transformationhydroquinone, homosalate, octisalate, zinc oxide | — | Kit | Obagi Cosmeceuticals LLC | 62032-912 | 62032-0912-01 |