NDC codes

FDA NDC Directory
Product NDC (as listed)85792-001Labeler and product segments. Claims need a package NDC.
Product NDC at billing width85792-0001Add 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
85792-001-01857920001018579200010130 mL in 1 BOX (85792-001-01)Marketed from Jun 20, 2025
85792-001-02857920001028579200010220 mL in 1 BOX (85792-001-02)Marketed from Jun 20, 2025
85792-001-03857920001038579200010315 mL in 1 BOX (85792-001-03)Marketed from Jun 20, 2025
85792-001-04857920001048579200010410 mL in 1 BOX (85792-001-04)Marketed from Jun 20, 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)
salicylic acid 17%
Active ingredients
Salicylic acid — 17 mg/mL
Dosage form
Liquid
Route
Topical
Labeler
Brilliance Trade LLCNDC labeler code 85792
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M 009
Marketing start
Listing expires
Identifiers
Product ID 85792-001_06a7b157-7cc9-4a5d-821c-c55e908687aaSPL ID 06a7b157-7cc9-4a5d-821c-c55e908687aaSPL set ID 377946a0-0e8c-70f4-e063-6294a90a1d85UNII O414PZ4LPZUPC 0199284961197

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

N485792000101 followed by a unit qualifier and the quantity

Package 85792-0001-01. 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)

For the removal of plantar wart common wart flat wart corn and callus

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85792-001

What is NDC 85792-001?
85792-001 is the product NDC for Bangbrek Bee Venom Wart Corn Callus Remover, Salicylic acid 17 mg/mL liquid, listed with the FDA by Brilliance Trade LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Bangbrek Bee Venom Wart Corn Callus Remover (Salicylic acid 17%).
What is the active ingredient?
Salicylic acid.
Who is the labeler?
Brilliance Trade LLC, NDC labeler code 85792. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bangbrek Bee Venom Wart Corn Callus 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 009

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

FDA NDC Directory listings under M 009
ProductStrengthForm · routeLabelerProduct NDC
Airmit AcedimenhydrinateDimenhydrinate 25 mg/1TabletOralSato Pharmaceutical Co., Ltd.49873-802
Allergy DyeFreeDiphenhydramine hydrochloride 25 mg/1Capsule, Liquid filledOralAllegiant Health69168-409
Boninemeclizine hydrochlorideMeclizine hydrochloride 25 mg/1Tablet, ChewableOralWellSpring Pharmaceutical Corporation65197-275
Boninemeclizine hydrochlorideMeclizine hydrochloride 25 mg/1Tablet, ChewableOralWellSpring Pharmaceutical Corporation65197-296
Boninemeclizine hydrochlorideMeclizine hydrochloride 25 mg/1Tablet, ChewableOralWellSpring Pharmaceutical Corporation65197-297
Bonine Maxmeclizine hydrochlorideMeclizine hydrochloride 50 mg/1Tablet, ChewableOralWellSpring Pharmaceutical Corporation65197-520
Childrens Allergydiphenhydramine hydrochlorideDiphenhydramine hydrochloride 12.5 mg/5mLLiquidOralDeMoulas Market Basket53942-505
CVS Motion Sickness Fast Meltingmeclizine hydrochlorideMeclizine hydrochloride 25 mg/1Tablet, Orally disintegratingOralCVS Pharmacy, Inc.59779-534
DimenhydrinateDimenhydrinate 50 mg/1TabletOralMajor Pharmaceuticals0904-6772
DimenhydrinateDimenhydrinate 50 mg/1TabletOralCVS Pharmacy, Inc.69842-206
DimenhydrinateDimenhydrinate 50 mg/1TabletOralLEADER/ Cardinal Health 110, Inc.70000-0404
Dramaminemeclizine hydrochlorideMeclizine hydrochloride 25 mg/1Tablet, ChewableOralMedtech Products Inc.63029-906
Dramaminemeclizine hydrochlorideMeclizine dihydrochloride 50 mg/1PowderOralMedtech Products Inc.63029-912
Dramaminemeclizine hydrochlorideMeclizine hydrochloride 25 mg/1Tablet, ChewableOralMedtech Products Inc.63029-913
Dramaminemeclizine hydrochlorideMeclizine hydrochloride 25 mg/1Tablet, ChewableOralMedtech Products Inc.63029-914
DramaminedimenhydrinateDimenhydrinate 50 mg/1Tablet, ChewableOralLil' Drug Store Products, Inc.66715-9809
Dramamine - Nmeclizine hydrochlorideMeclizine hydrochloride 25 mg/1TabletOralMedtech Products Inc.63029-905
Dramamine Chewable Orangemeclizine hydrochlorideMeclizine hydrochloride 25 mg/1Tablet, ChewableOralMedtech Products Inc.63029-915
Dramamine for KidsdimenhydrinateDimenhydrinate 25 mg/1Tablet, ChewableOralMedtech Products Inc.63029-904
Dramamine for KidsdimenhydrinateDimenhydrinate 25 mg/1Tablet, ChewableOralMedtech Products Inc.63029-908

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