NDC codes

FDA NDC Directory
Product NDC (as listed)24909-051Labeler and product segments. Claims need a package NDC.
Product NDC at billing width24909-0051Add 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
24909-051-142490900511414 g in 1 TUBE (24909-051-14)Marketed from Sep 22, 2025

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

Generic name (nonproprietary)
graphite 10x, natrum muriaticum 3x, symphytum officinale (comfrey) 1x, thuja occidentalis 3x
Active ingredients
Sodium chloride — 3 [hp_X]/gSymphytum officinale whole — 1 [hp_X]/gThuja occidentalis leafy twig — 3 [hp_X]/gGraphite — 10 [hp_X]/g
Dosage form
Ointment
Route
Topical
Labeler
Aidance Scientific, Inc.NDC labeler code 24909
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 24909-051_3d367c0f-5a29-eded-e063-6394a90ad2dcSPL ID 3d367c0f-5a29-eded-e063-6394a90ad2dcSPL set ID 3d367c0f-5a28-eded-e063-6394a90ad2dcUNII 451W47IQ8X, H8FJJ6KX5Y, 1NT28V9397, 4QQN74LH4O

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

N424909005114 followed by a unit qualifier and the quantity

Package 24909-0051-14. 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 the relief of symptoms associated with warts.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 24909-051

What is NDC 24909-051?
24909-051 is the product NDC for terrasil Fast and Natural Wart Removal, Sodium chloride 3 [hp_X]/g + 3 more ingredients ointment, listed with the FDA by Aidance Scientific, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
terrasil Fast and Natural Wart Removal (Graphite 10X, Natrum Muriaticum 3X, Symphytum Officinale (Comfrey) 1X, Thuja Occidentalis 3X).
What is the active ingredient?
Sodium chloride, Symphytum officinale whole, Thuja occidentalis leafy twig, Graphite.
Who is the labeler?
Aidance Scientific, Inc., NDC labeler code 24909. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for terrasil Fast and Natural Wart Removal?
1 other product NDC are listed under this name. See all terrasil Fast and Natural Wart Removal NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other terrasil Fast and Natural Wart Removal NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Terrasil Fast and Natural Wart Removalthuja occidentalisThuja occidentalis leafy twig 6 [hp_X]/gOintmentTopicalAidance Skincare & Topical Solutions, LLC24909-16124909-0161-15

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