What is NDC 59088-328?

59088-328 is the product NDC for Hydroxate Gel (hydrocortisone 2%), Hydrocortisone 20 mg/g gel, listed with the FDA by PureTek Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Hydroxate Gel (Hydrocortisone 2%).

PureTek Corporation, NDC labeler code 59088. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Hydroxate Gel?

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.

Hydroxate Gel NDC 59088-328 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-328Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0328Add 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 NDC	11-digit (billing)	Package	Copy
59088-328-03	59088032803	28 g in 1 TUBE (59088-328-03)Marketed from Mar 15, 2024

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): Hydroxate Gel
Generic name (nonproprietary): hydrocortisone 2%
Active ingredients: Hydrocortisone — 20 mg/g
Dosage form: Gel
Route: Topical
Labeler: PureTek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Mar 15, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 59088-328_13bc5f75-b5ca-4d48-e063-6394a90ab608SPL ID 13bc5f75-b5ca-4d48-e063-6394a90ab608SPL set ID 13bc5f75-b5cb-4d48-e063-6394a90ab608RxCUI 604449UNII WI4X0X7BPJ
Pharmacologic class: Corticosteroid

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 HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N459088032803 followed by a unit qualifier and the quantity

Package 59088-0328-03. 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 Mar 15, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Topical corticosteroids are indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatosis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59088-328

What is NDC 59088-328?: 59088-328 is the product NDC for Hydroxate Gel (hydrocortisone 2%), Hydrocortisone 20 mg/g gel, listed with the FDA by PureTek Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Hydroxate Gel (Hydrocortisone 2%).
What is the active ingredient?: Hydrocortisone.
Who is the labeler?: PureTek Corporation, NDC labeler code 59088. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Hydroxate Gel?: 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.

Hydroxate Gel (Hydrocortisone 2%) NDC 59088-328