NDC codes

FDA NDC Directory
Product NDC (as listed)85569-018Labeler and product segments. Claims need a package NDC.
Product NDC at billing width85569-0018Add 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
85569-018-01855690018018556900180115 g in 1 CARTON (85569-018-01)Marketed from Oct 7, 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)
Treatonic Wart Remover
Generic name (nonproprietary)
salicylic acid 12%
Active ingredients
Salicylic acid — 12 g/100g
Dosage form
Liquid
Route
Topical
Labeler
100 KARMA INCNDC labeler code 85569
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M 018
Marketing start
Listing expires
Identifiers
Product ID 85569-018_5b90cc91-6eff-1bdb-e063-6394a90a6198SPL ID 5b90cc91-6eff-1bdb-e063-6394a90a6198

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

N485569001801 followed by a unit qualifier and the quantity

Package 85569-0018-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 85569-018

What is NDC 85569-018?
85569-018 is the product NDC for Treatonic Wart Remover (salicylic acid 12%), Salicylic acid 12 g/100g liquid, listed with the FDA by 100 KARMA INC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Treatonic Wart Remover (Salicylic Acid 12%).
What is the active ingredient?
Salicylic acid.
Who is the labeler?
100 KARMA INC, NDC labeler code 85569. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Treatonic 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.

Other NDCs under M 018

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

FDA NDC Directory listings under M 018
ProductStrengthForm · routeLabelerProduct NDC
Advanced Eye Relief Dry Eye Rejuvenationglycerin propylene glycolGlycerin 3 mg/mL; Propylene glycol 10 mg/mLSolution/ dropsOphthalmicBausch & Lomb Incorporated24208-454
Advanced Eye Relief Eye Washwater solutionWater 99.05 mL/100mLSolution/ dropsOphthalmicBausch & Lomb Incorporated24208-005
Advanced Eye Relief/ Redness Maximum Reliefnaphazoline hydrochloride and hypromelloseHypromellose, Unspecified 5 mg/mL; Naphazoline hydrochloride .3 mg/mLSolution/ dropsOphthalmicBausch & Lomb Incorporated24208-450
Alcon Tears Lubricant Eye Dropshypromellose 2910Hypromellose 2910 (4000 mpa.s) 5 mg/mLSolution/ dropsOphthalmicAlcon Laboratories, Inc.0065-0408
Altachlore Sodium Chloride Hypertonicitysodium chlorideSodium chloride 50 mg/mLSolution/ dropsOphthalmicAltaire Pharmaceuticals Inc.59390-183
Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percentsodium chlorideSodium chloride 50 mg/gOintmentOphthalmicAltaire Pharmaceuticals Inc.59390-184
Altalubemineral oil and petrolatumMineral oil 150 mg/g; Petrolatum 850 mg/gOintmentOphthalmicAltaire Pharmaceuticals Inc.59390-198
Ancient Secrets Breathe Againsodium chlorideSodium chloride 20 mg/100mLAerosol, SprayNasalLOTUS BRANDS, INC.76328-100
Archies Dry Eye Reliefpolyethylene glycol 400, propylene glycolPolyethylene glycol 400 .4 g/100mL; Propylene glycol .3 g/100mLSolution/ dropsOphthalmicArchie's Remedies83737-001
Artifical Tearsglycerin and propylene glycolGlycerin 3 mg/mL; Propylene glycol 10 mg/mLSolution/ dropsOphthalmicWal-Mart Stores Inc49035-454
Artificial TearsDextran 70 1 mg/mL + 2 more ingredientsSolution/ dropsOphthalmicAvPAK50268-043
Artificial Tearspolyvinyl alcohol, povidonePovidone, Unspecified 6 mg/mL; Polyvinyl alcohol, Unspecified 5 mg/mLSolution/ dropsOphthalmicKC Pharmaceuticals, Inc.55651-008
Artificial TearsglycerinGlycerin .002 mg/mg + 2 more ingredientsSolution/ dropsOphthalmicGeri-Care Pharmaceuticals, Corp57896-181
Artificial TearsglycerinGlycerin .002 mg/mg + 2 more ingredientsSolution/ dropsOphthalmicNuCare Pharmaceuticals,Inc.68071-4555
Artificial Tearspolyvinyl alcohol, povidonePolyvinyl alcohol, Unspecified .5 g/100mL; Povidone .6 g/100mLSolutionOphthalmicNuCare Pharmaceuticals,Inc.68071-4914
Artificial Tears Lubricant Eye Dropsglycerin, hypromellose, polyethylene glycol 400Glycerin .2 g/100mL + 2 more ingredientsSolution/ dropsOphthalmicKC Pharmaceuticals, Inc55651-115
Artificial Tears Lubricant Eye Dropsglycerin, propylene glycolGlycerin 3 mg/mL; Propylene glycol 10 mg/mLSolution/ dropsOphthalmicCVS Pharmacy69842-454
Auro-Cmccarboxymethylcellulose eye drops 0.5%Carboxymethylcellulose sodium, Unspecified 5 mg/mLFor solutionTopicalAurolab16030-401
Aurodone Povidone Iodine 5 % Opthalmic Solutionpovidone iodine 5 % topical solutionPovidone-iodine 5 mg/mLSolutionTopicalAurolab16030-601
Aurovischypromellose ophthalmic solution 2% w/vHypromellose 2208 (15000 mpa.s) 20 mg/mLSolutionOphthalmicAurolab16030-301

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