NDC codes

FDA NDC Directory
Product NDC (as listed)10738-073Labeler and product segments. Claims need a package NDC.
Product NDC at billing width10738-0073Add 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
10738-073-21107380073211073800732157 g in 1 JAR (10738-073-21)Marketed from Aug 30, 2019
10738-073-411073800734110738007341113 g in 1 JAR (10738-073-41)Marketed from Aug 30, 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)
Triderma Pain Relief
Generic name (nonproprietary)
lidocaine hcl, menthol
Active ingredients
Lidocaine hydrochloride — 4 g/100gMenthol, Unspecified form — 1 g/100g
Dosage form
Cream
Route
Topical
Labeler
Genuine Virgin Aloe CorporationNDC labeler code 10738
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication 505G(a)(3)
Marketing start
Listing expires
Other FDA classes
Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers
Product ID 10738-073_496701e3-f506-de4f-e063-6294a90a70ffSPL ID 496701e3-f506-de4f-e063-6294a90a70ffSPL set ID 9172d6cd-f7d3-421e-a8b5-c1cb3325ada5RxCUI 1595624UNII V13007Z41A, L7T10EIP3AUPC 0182228000410, 0818926013260
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

N410738007321 followed by a unit qualifier and the quantity

Package 10738-0073-21. 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 For temporary relief of pain

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 10738-073

What is NDC 10738-073?
10738-073 is the product NDC for Triderma Pain Relief, Lidocaine hydrochloride 4 g/100g; Menthol, Unspecified form 1 g/100g cream, listed with the FDA by Genuine Virgin Aloe Corporation. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Triderma Pain Relief (Lidocaine HCl, Menthol).
What is the active ingredient?
Lidocaine hydrochloride, Menthol, Unspecified form.
Who is the labeler?
Genuine Virgin Aloe Corporation, NDC labeler code 10738. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Triderma Pain Relief?
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.

Other NDCs under 505G(a)(3)

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under 505G(a)(3)
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Smart Care SWEET AND STILL HAND SANITIZERethyl alcoholAlcohol 70 mL/100mLSprayTopicalAshtel Studios, Inc.70108-192
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