Over-the-counter drug · UNAPPROVED DRUG OTHER
Obagi Nu-Derm FX System Normal - Dry Skin Transformation Complexion Brightening System (Homosalate, octisalate, and zinc oxide) NDC 62032-539
Kit · Obagi Cosmeceuticals LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 62032-539-07 | 62032053907 | 1 KIT in 1 CARTON (62032-539-07) * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 48 g in 1 BOTTLE, PLASTIC * 85 g in 1 TUBE * 57 g in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTICMarketed from Dec 2, 2019 |
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 FX System Normal - Dry Skin Transformation Complexion Brightening SystemSuffix: Skin Transformation Complexion Brightening System
- Generic name (nonproprietary)
- homosalate, octisalate, and 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 62032-539_0ad34be9-6f0d-446b-8131-94f8e5f453b9SPL ID 0ad34be9-6f0d-446b-8131-94f8e5f453b9SPL set ID 512b20f0-60c8-47d4-a732-22fc999980d3
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
N462032053907followed by a unit qualifier and the quantityPackage 62032-0539-07. 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 62032-539
- What is NDC 62032-539?
- 62032-539 is the product NDC for Obagi Nu-Derm FX System Normal - Dry Skin Transformation Complexion Brightening System 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 FX System Normal - Dry Skin Transformation Complexion Brightening System (Homosalate, Octisalate, and 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 FX System Normal - Dry Skin Transformation Complexion Brightening System?
- 1 other product NDC are listed under this name. See all Obagi Nu-Derm FX System Normal - Dry Skin Transformation Complexion Brightening System 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 FX System Normal - Dry Skin Transformation Complexion Brightening System 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 Fx System Normal-Dry Skin Transformation Complexion Brightening Systemtitanium dioxide, zinc oxide | — | Kit | Obagi Cosmeceuticals LLC | 62032-924 | 62032-0924-01 |