What is NDC 62032-917?

62032-917 is the product NDC for Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin kit, listed with the FDA by Obagi Cosmeceuticals LLC.

What drug is associated with this NDC?

Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin (Homosalate, Octisalate, Zinc oxide).

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-C Fx System Normal-Oily Skin Brightening System with Arbutin?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

NDC 62032-917

NDC codes

FDA NDC Directory

Product NDC (as listed)62032-917Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62032-0917Add the package segment from the table below.

Product information

Brand name (proprietary): Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin
Generic name (nonproprietary): homosalate, octisalate, 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: Dec 2, 2019
Listing expires: Dec 31, 2027
Identifiers: Product ID 62032-917_a27a6106-f8cb-47e4-8e71-1f7dceb77d3dSPL ID a27a6106-f8cb-47e4-8e71-1f7dceb77d3dSPL set ID 321e58d0-9964-4da9-af6b-66ba81b60cf7

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.

Product label

Current FDA label (SPL), effective Jan 26, 2026.

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.

Full label on DailyMed (opens in a new tab)

About NDC 62032-917

What is NDC 62032-917?: 62032-917 is the product NDC for Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin kit, listed with the FDA by Obagi Cosmeceuticals LLC.
What drug is associated with this NDC?: Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin (Homosalate, Octisalate, 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-C Fx System Normal-Oily Skin Brightening System with Arbutin?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin (Homosalate, octisalate, zinc oxide) NDC 62032-917