NDC codes

FDA NDC Directory
Product NDC (as listed)85779-005Labeler and product segments. Claims need a package NDC.
Product NDC at billing width85779-0005Add 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
85779-005-01857790005018577900050130 mL in 1 BOTTLE (85779-005-01)Marketed from Aug 19, 2026

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)
Txovis SKIN WART CORN REMOVER
Generic name (nonproprietary)
salicylic acid
Active ingredients
Salicylic acid — 40 mg/100mL
Dosage form
Liquid
Route
Topical
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication 505G(a)(3)
Marketing start
Listing expires
Identifiers
Product ID 85779-005_596226a3-a27a-288b-e063-6394a90abc35SPL ID 596226a3-a27a-288b-e063-6394a90abc35SPL set ID 596226a3-a279-288b-e063-6394a90abc35UNII O414PZ4LPZ

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

N485779000501 followed by a unit qualifier and the quantity

Package 85779-0005-01. 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 .

Indications (excerpt from the label)

Wash affected area and dry thoroughly.Apply a small amount at a time with the applicatorto sufficiently cover each wart. Let dry.Repeat once or twice daily as needed until thewart is removed,for up to 12 weeks

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85779-005

What is NDC 85779-005?
85779-005 is the product NDC for Txovis SKIN WART CORN REMOVER (salicylic acid), Salicylic acid 40 mg/100mL liquid, listed with the FDA by Guangdong Joyan Biological Technology Co.,Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Txovis SKIN WART CORN REMOVER (Salicylic acid).
What is the active ingredient?
Salicylic acid.
Who is the labeler?
Guangdong Joyan Biological Technology Co.,Ltd, NDC labeler code 85779. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Txovis SKIN WART CORN 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.

Other NDCs under 505G(a)(3)

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

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Chemstation HACCP Q E2benzalkonium chlorideBenzalkonium chloride 1.2 g/LLiquidTopicalChemStation71212-101
Antibacterial Hand SanitizeralcoholAlcohol 620 mg/mLSprayTopicalTEKWELD SOLUTIONS, INC.71160-189
VQ Hydrating Hand Sanitizer Spiced PumpkinalcoholAlcohol 70 mL/100mLLiquidTopicalTychea Co.85980-014
Bcbgeneration 4 Pc Hand Sanitizers - Cherry Blossom, Brown Sugar Vanilla, Velvet Peach And Ocean Breeze Scentethyl alcohol—KitDiamond Life Cosmetics Trading FZCO87247-590

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