NDC codes

FDA NDC Directory
Product NDC (as listed)62032-912Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62032-0912Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
62032-912-0162032091201620320912011 KIT in 1 CARTON (62032-912-01) * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 57 g in 1 BOTTLE, PLASTIC (62032-100-36) * 48 g in 1 BOTTLE, PLASTIC * 1 TUBE in 1 CARTON (62032-140-09) / 85 g in 1 TUBE * 198 mL in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTICMarketed from Jun 25, 2021

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

Generic name (nonproprietary)
hydroquinone, homosalate, octisalate, zinc oxide
Dosage form
Kit
Labeler
Obagi Cosmeceuticals LLCNDC labeler code 62032
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 62032-912_76f5663b-4048-4b30-ad97-692294b81a7cSPL ID 76f5663b-4048-4b30-ad97-692294b81a7cSPL set ID e63327db-fb96-411c-945a-abe801d38045RxCUI 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

N462032091201 followed by a unit qualifier and the quantity

Package 62032-0912-01. 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.

Full label on DailyMed (opens in a new tab)

About NDC 62032-912

What is NDC 62032-912?
62032-912 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, 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 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.

Other finished products listed under the same name: strengths, forms and labelers.

Other Obagi Nu-Derm System Normal-Oily Skin Transformation NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Obagi Nu-Derm System Normal-Oily Skin Transformationhydroquinone, titanium dioxide, zinc oxide—KitObagi Cosmeceuticals LLC62032-91962032-0919-01

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