Home › NDC Lookup › Ingredients › Salicylic Acid, Chlorhexidine › 84288-0005-01
Wart Remover SALICYLIC ACID, CHLORHEXIDINE 1 g/100g; 1 g/100g Ointment, 20 g — NDC 84288-0005-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Wart Remover SALICYLIC ACID, CHLORHEXIDINE 1 g/100g; 1 g/100g Ointment, 20 g — NDC 84288-005-01 (Billing 84288-0005-01)

by Dongkou County Hecheng Network Technology Co., Ltd. · 20 g in 1 TUBE

This is a package of 20 g of Wart Remover SALICYLIC ACID, CHLORHEXIDINE 1 g/100g; 1 g/100g Ointment from Dongkou County Hecheng Network Technology Co., Ltd., marketed since Aug 2024 and currently FDA-listed. It is this product's only package size.

NDC 84288-0005-01
🏷️ FDA NDC (as labeled) 84288-005-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 84288-005-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
84288 labeler · 005 product · 01 package
Package marketed since
Aug 2, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
6932511224702
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84288-005-01
Product NDC 84288-005
11-digit billing NDC 84288000501
RxCUI 2682584
UNII O414PZ4LPZ, R4KO0DY52L
UPC 6932511224702
Application # M028
SPL Set ID 1eaf21d0-492b-8764-e063-6394a90a6188
Physiologic effect Decreased Cell Wall Integrity
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-08-02
Route TOPICAL
Dosage form OINTMENT
Substance SALICYLIC ACID; CHLORHEXIDINE
Quick answers
  • RxCUI (RxNorm): 2682584
Why two NDCs? The FDA registers this code as 84288-005-01 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 84288-0005-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

RxNorm drug class

This medicine belongs to the Antiinfectives and antiseptics for local oral treatment class.

Drug family (ATC) Antiinfectives and antiseptics for local oral treatment, Antiinfectives, Biguanides and amidines
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

🧪 What is this product?

This is a topical ointment marketed as an over-the-counter wart remover under FDA's OTC monograph rules. It contains salicylic acid, which is typically used to help soften and remove thickened skin, and chlorhexidine, an antiseptic commonly used to help reduce bacteria on the skin. The two ingredients are combined in a single formulation intended for application directly to the affected area.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer gPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
84288-0005-01 You're viewing this Main listing 20 g in 1 TUBE 2024-08-02 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Wart Remover Ointmen t 1 g/100g; 1 g/100g 84288-0001-01 Dongkou 20 g — — FDA listed —
Wart Remover 1 g/100g; 1 g/100gthis 84288-0005-01 Dongkou 20 g — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2024
On the market since
Aug 2024
📍
2026
Currently FDA-listed
2 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII 1V63N2S972
    A plant extract from angelica dahurica root used in traditional formulations. It may function as a flavoring agent, fragrance component, or natural ingredient to add therapeutic appeal to the medicine.
  • UNII 73070DU1LA
    Arctium lappa, or burdock root, is a plant extract used as a natural flavoring agent and potential color component in some medicines. It may help mask bitter tastes and add mild flavor to oral formulations.
  • UNII T1134STW1K
    A plant extract derived from Asarum sieboldii, used in some formulations as a flavoring agent or traditional ingredient to add taste or aroma to the medicine.
  • UNII 08T3N29QJB
    A plant-derived ingredient from atractylodes root, traditionally used in herbal formulations. It may function as a binder or filler to hold tablet ingredients together or add bulk to the medicine.
  • UNII EMY54R518C
    A natural extract from bamboo leaves used as a filler and thickening agent in medications. It helps give the product proper texture and consistency while serving as a plant-based inactive ingredient.
  • UNII M89NIB437X
    Borneol is a waxy, plant-derived alcohol obtained from camphor trees or made synthetically. It's used in medicines as a flavoring agent and penetration enhancer to improve how active ingredients are absorbed.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII O0OX7CMF92
    A plant extract from mandarin oranges used as a natural flavoring and fragrance ingredient. It adds citrus taste and aroma to medicines, making them more pleasant to take.
  • UNII V1IA3S3CUS
    A plant extract derived from Cnidium monnieri fruit, commonly used in traditional Asian medicine preparations. In formulations, it may serve as an active botanical ingredient or flavoring agent, though its specific role depends on the product type.
  • UNII YM9E56VP46
    Forsythia suspensa root is a plant-derived ingredient used in traditional formulations. It may serve as a natural flavoring, colorant, or texture modifier in the medicine.
  • UNII Y9H1V576FH
    Honey is a natural sweetener made by bees from flower nectar. In medicines, it adds sweetness to improve taste and may help soothe throat irritation in lozenges or syrups.
  • UNII WC73QE9274
    A plant extract from balloon flower root used in traditional Asian medicine. It functions as a flavoring agent and natural ingredient to support the formulation's taste and herbal profile.
  • UNII D5J3623SV2
    Portulaca oleracea is a plant extract used in medicines as a natural ingredient. It may function as an antioxidant or skin-conditioning agent in topical formulations.
  • UNII IYR6K8KQ5K
    A plant extract from sophora flavescens root used as a natural colorant and flavoring agent in medicines. It may also help preserve the product and provide texture.

15 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesANGELICA DAHURICA ROOT CITRUS RETICULATA WHOLE FORSYTHIA SUSPENSA ROOT PLATYCODON GRANDIFLORUS WHOLE ASARUM SIEBOLDII CETOSTEARYL ALCOHOL SOPHORA FLAVESCENS ROOT PORTULACA OLERACEA WHOLE ATRACTYLODES MACROCEPHALA ROOT ARCTIUM LAPPA WHOLE BAMBUSA VULGARIS LEAF BORNEOL CNIDIUM MONNIERI FRUIT HONEY ALCOHOL

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerDongkou County Hecheng Network Technology Co., Ltd.
FDA applicationM028 (OTC MONOGRAPH DRUG)
Labeler code84288
First marketedAug 2024
Product typeHuman Otc Drug
Portfolio7 products on file

More NDCs from Dongkou County Hecheng Network Technology Co., L... labeler code 84288

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 26 words ▾

After cleansing the areas to betreat-edwithlukewarm water,apply proper amou-ntofthecream to the surface of theaffectedareaandgentlyrub infor 5-10 minutes untilit is fullyabsorbed.itisrecommendedtousethis productcontinuously2-3 times aday un-til the wartsfalloff.

⏱️ Dosage and Administration 53 words ▾

wash the affected area may soak the wart in warm water for 5minutes dry area thoroughly using the applicator(cotton swab),apply alayer of ointment to sufficiently cover eachwart allow it to fully absorb and cover it with cbandage as needed. repeat this procedure once ortwicedailyas needed (until the wart isremoved) for upto 12 weeks

⚠️ Warnings 10 words ▾

For external use only. Keep away from fire and flame

📦 Storage and Handling 7 words ▾

Store in a dry and cool place

🧪 Active Ingredient 5 words ▾

SALICYLIC ACID 1% CHLORHEXIDINE 1%

🧪 Inactive Ingredients 37 words ▾

ANGELICA DAHURICA ROOT CITRUS RETICULATA WHOLE FORSYTHIA SUSPENSA ROOT PLATYCODON GRANDIFLORUS WHOLE ASARUM SIEBOLDII CETOSTEARYL ALCOHOL SOPHORA FLAVESCENS ROOT PORTULACA OLERACEA WHOLE ATRACTYLODES MACROCEPHALA ROOT ARCTIUM LAPPA WHOLE BAMBUSA VULGARIS LEAF BORNEOL CNIDIUM MONNIERI FRUIT HONEY ALCOHOL

🎯 Purpose 2 words ▾

wart Remove

📄 Keep Out of Reach of Children 11 words ▾

Keep out of reach of childrenIfswallowed, get medical help orcontacta Poisoncontrolcenter(1-800-222-1222)rightaway

📄 Package Label / Principal Display Panel 2 words ▾

label label2

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Dongkou County Hecheng Network Technology Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Dongkou County Hecheng Network Technology Co., Ltd. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 84288-0004-01 · Dongkou 84288-0006-01 · Dongkou →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.