What is NDC 70463-725?

70463-725 is the product NDC for SOMXL Homeopathic Wart Remover (thuja occidentalis leafy twig), Thuja occidentalis leafy twig 6 [hp_X]/15g cream, listed with the FDA by WR Group Skin Care Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

SOMXL Homeopathic Wart Remover (Thuja occidentalis leafy twig).

WR Group Skin Care Ltd, NDC labeler code 70463. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for SOMXL Homeopathic Wart Remover?

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.

SOMXL Homeopathic Wart Remover NDC 70463-725

NDC codes

FDA NDC Directory

Product NDC (as listed)70463-725Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70463-0725Add 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
70463-725-01	70463072501	1 TUBE in 1 BOX (70463-725-01) / 15 g in 1 TUBEMarketed from Feb 5, 2016

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): SOMXL Homeopathic Wart Remover
Generic name (nonproprietary): thuja occidentalis leafy twig
Active ingredients: Thuja occidentalis leafy twig — 6 [hp_X]/15g
Dosage form: Cream
Route: Topical
Labeler: WR Group Skin Care LtdNDC labeler code 70463
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 5, 2016
Listing expires: Dec 31, 2026
Identifiers: Product ID 70463-725_2f76aa11-04fe-8c60-e063-6294a90a5470SPL ID 2f76aa11-04fe-8c60-e063-6294a90a5470SPL set ID 63e48a74-0efd-4ebe-a5c6-cbdfd6b9c0c8UNII 1NT28V9397

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

N470463072501 followed by a unit qualifier and the quantity

Package 70463-0725-01. 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 Mar 3, 2025.

Indications (excerpt from the label)

Use For the removal of common warts. The common wart is easily recognized by the rough “cauliflower-like” appearance on the surface.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70463-725

What is NDC 70463-725?: 70463-725 is the product NDC for SOMXL Homeopathic Wart Remover (thuja occidentalis leafy twig), Thuja occidentalis leafy twig 6 [hp_X]/15g cream, listed with the FDA by WR Group Skin Care Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: SOMXL Homeopathic Wart Remover (Thuja occidentalis leafy twig).
What is the active ingredient?: Thuja occidentalis leafy twig.
Who is the labeler?: WR Group Skin Care Ltd, NDC labeler code 70463. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for SOMXL Homeopathic Wart Remover?: 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.

SOMXL Homeopathic Wart Remover (Thuja occidentalis leafy twig) NDC 70463-725