Triderma Bruise Defense Healing -Diabetics NDC 10738-065

NDC codes

FDA NDC Directory

Product NDC (as listed)10738-065Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10738-0065Add 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
10738-065-40	10738006540	1 TUBE in 1 CARTON (10738-065-40) / 119 g in 1 TUBE (10738-065-45)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 Bruise Defense Healing -Diabetics
Generic name (nonproprietary): arnica montana flower extract
Active ingredients: Arnica montana flower — 1.6 g/100g
Dosage form: Cream
Route: Topical
Labeler: Genuine Virgin Aloe Corporation
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 30, 2019
Listing expires: Dec 31, 2027
Identifiers: Product ID 10738-065_4977f4b0-cc80-a8a4-e063-6394a90a00a8SPL ID 4977f4b0-cc80-a8a4-e063-6394a90a00a8SPL set ID 6e772fc2-8ba6-4a6a-9856-ca70470a4f03UNII OZ0E5Y15PZUPC 0818926010177

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

N410738006540 followed by a unit qualifier and the quantity

Package 10738-0065-40. 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 28, 2026.

Indications (excerpt from the label)

Uses • Temporarily relieves muscle pain and stiffness due to minor injuries, overexertion and falls • Reduces pain, swelling and discoloration from bruises

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)