What is NDC 59088-475?

59088-475 is the product NDC for Lidorex (lidocaine hcl), Lidocaine hydrochloride 28 mg/g gel, listed with the FDA by PureTek Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.

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 Lidorex?

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.

Lidorex NDC 59088-475 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-475Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0475Add 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
59088-475-07	5908804750759088047507	100 g in 1 TUBE (59088-475-07)Marketed from Oct 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

Brand name (proprietary): Lidorex
Generic name (nonproprietary): lidocaine hcl
Active ingredients: Lidocaine hydrochloride — 28 mg/g
Dosage form: Gel
Route: Topical
Labeler: PureTek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Oct 25, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers: Product ID 59088-475_f2051c68-cdd9-58b2-e053-2995a90a6b48SPL ID f2051c68-cdd9-58b2-e053-2995a90a6b48SPL set ID cc9eeba3-695d-d14e-e053-2a95a90a5c03RxCUI 2562183UNII V13007Z41AUPC 0359088475072
Pharmacologic class: Amide Local Anesthetic; Antiarrhythmic

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

N459088047507 followed by a unit qualifier and the quantity

Package 59088-0475-07. 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 Jan 11, 2023.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritation.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59088-475

What is NDC 59088-475?: 59088-475 is the product NDC for Lidorex (lidocaine hcl), Lidocaine hydrochloride 28 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?: Lidorex (Lidocaine HCl).
What is the active ingredient?: Lidocaine hydrochloride.
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 Lidorex?: 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.

Lidorex (Lidocaine hcl) NDC 59088-475