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Ladoverna Salicylic Acid Solution 17 g/100mL Solution, 30 mL — NDC 85772-0011-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Ladoverna Salicylic Acid Solution 17 g/100mL Solution, 30 mL — NDC 85772-0011-1 (Billing 85772-0011-01)

by Guangzhou Oupeng Cosmetics Co., Ltd. · 1 BOX in 1 CARTON / 30 mL in 1 BOX

This is a package of 30 mL of Ladoverna Salicylic Acid Solution 17 g/100mL Solution from Guangzhou Oupeng Cosmetics Co., Ltd., marketed since Jul 2026 and currently FDA-listed. It is this product's only package size.

NDC 85772-0011-01
🏷️ FDA NDC (as labeled) 85772-0011-1 billing pads the package 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 85772-0011-1
Product NDC 85772-0011
11-digit billing NDC 85772001101
RxCUI 312881
UNII O414PZ4LPZ
Application # M028
SPL Set ID 55ea1515-b4f1-5d7d-e063-6394a90ab7bc
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-07-06
Route TOPICAL
Dosage form SOLUTION
Substance SALICYLIC ACID
Quick answers
  • RxCUI (RxNorm): 312881
Why two NDCs? The FDA registers this code as 85772-0011-1 — a 5-4-1 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 package segment → 85772-0011-01. 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 Salicylic acid and derivatives class.

Drug family (ATC) Salicylic acid and derivatives, Other antifungals for topical use, Antiinflammatory agents, non-steroids
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

📖 About the active ingredient: Salicylic Acid MedlinePlus · NLM
General information about the ingredient itself — the description of this specific product follows below.

Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions that involve scaling or overgrowth of skin cells such as psoriasis (a skin disease in which red, scaly patches form on some areas of the body), ichthyoses (inborn conditions that cause skin dryness and scaling), dandruff, corns, calluses, and warts on the hands or feet. Topical salicylic acid should not be used to treat genital warts, warts on the face, warts with hair growing from them, warts in the nose or mouth, moles, or b...

Read the full MedlinePlus article ↗
🧪 What is this product?

Ladoverna Salicylic Acid Solution is a topical liquid product containing 17 percent salicylic acid. Salicylic acid is a keratolytic agent commonly used in over-the-counter skincare products to help soften and remove dead skin cells. This is an OTC monograph drug, meaning it is marketed under FDA's established rules for its product category rather than as an individually approved application.

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 mLPer 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
85772-0011-01 You're viewing this Main listing 1 BOX in 1 CARTON / 30 mL in 1 BOX 2026-07-07 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Ladoverna 17 g/100mLthis 85772-0011-01 Guangzhou 30 ml — — 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

🏛️
2026
On the market since
Jul 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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.

What it looks like

Color yellow
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

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.

  • 1.5 mL / 100 mL UNII TR046Y3K1G
    A liquid alcohol derived from petroleum or plant sources. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • 45 mL / 100 mL 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.
  • 0.05 mL / 100 mL UNII 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • 0.1 mL / 100 mL UNII 94ZLA3W45F
    Arginine is an amino acid used in medicines as a buffer and pH adjuster. It helps maintain the proper acidity level and stability of liquid formulations.
  • 0.05 mL / 100 mL UNII 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • 4 mL / 100 mL UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • 0.0035 mL / 100 mL UNII J1M3NA843L
    A spicy pepper extract used as a flavoring agent in medicines. It adds taste to mask bitter drug flavors and improve palatability, especially in liquid or chewable formulations.
  • 0.1 mL / 100 mL UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • 0.0028 mL / 100 mL UNII GXZ33VNT92
    Gentiana scabra root is a plant extract used in some formulations as a flavoring agent and natural colorant. It may also serve to support the product's stability and shelf life.
  • 0.0025 mL / 100 mL UNII CHC1JS541R
    A plant extract from gynostemma pentaphyllum, also called jiaogulan. It's used in supplements and some medicines as a filler or botanical ingredient to add volume and potential bioactive compounds to the formulation.
  • 0.005 mL / 100 mL UNII S270N0TRQY
    Hyaluronic acid is a naturally occurring substance found in skin and joints. In medicines, it acts as a moisturizer and thickening agent to improve texture and help the product spread smoothly.
  • 0.35 mL / 100 mL UNII G1L3HT4CMH
    A synthetic compound used in medicines as a preservative and antimicrobial agent. It helps prevent bacterial and fungal growth, extending the product's shelf life.
  • 0.02 mL / 100 mL UNII 2BF9E65L7I
    A chemical compound combining menthol with lactic acid. It's used in medicines as a flavoring agent and to provide a cooling or soothing sensation on the skin or mouth.
  • 1 mL / 100 mL UNII 7YC686GQ8F
    A synthetic oily substance made from castor oil. It works as a solubilizer and emulsifier to help mix oily and water-based ingredients together in the medicine.
  • 0.12 mL / 100 mL UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • 0.002 mL / 100 mL UNII BOW48C81XP
    A plant extract from the kava root, used as a flavoring agent to add taste to medicines. It may also help mask bitter flavors in oral formulations.
  • 5 mL / 100 mL UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • 0.0022 mL / 100 mL 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.
  • 0.001 mL / 100 mL UNII 48PS81XHK0
    A plant-derived ingredient from the root of Stephania tetrandra, a climbing vine used in traditional medicine. In formulations, it may function as a natural extract or botanical filler.
  • 0.003 mL / 100 mL UNII 7DQZ24B35Y
    A plant-derived substance from the Vincetoxicum atratum root used in traditional formulations. It may function as a binder or filler to help hold tablet ingredients together or add bulk to the dosage form.
  • 25.6762 mL / 100 mL UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • 0.01 mL / 100 mL UNII 44FQ49X6UN
    A polysaccharide (complex carbohydrate) derived from yeast cell walls. In medicines, it acts as a binder to hold tablet ingredients together and may help with tablet structure and stability.
  • 0.0018 mL / 100 mL UNII 3CIP16A418
    A plant extract from Sichuan pepper fruit used as a flavoring agent and natural fragrance component in medicines. It adds taste and aroma to make medications more palatable.

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

The official label also states1,2-HEXANEDIOL, ALCOHOL, ALLANTOIN, ARGININE, BISABOLOL, BUTYLENE GLYCOL, CAPSICUM FRUTESCENS FRUIT EXTRACT, CYNANCHUM ATRATUM EXTRACT, ETHYLHEXYLGLYCERIN, GENTIANA SCABRA ROOT EXTRACT, GYNOSTEMMA PENTAPHYLLUM EXTRACT, HYALURONIC ACID, HYDROXYACETOPHENONE, MENTHYL LACTATE, PEG-40 HYDROGENATED CASTOR OIL, PHENOXYETHANOL, PIPER METHYSTICUM ROOT EXTRACT, PROPYLENE GLYCOL, SOPHORA ANGUSTIFOLIA ROOT EXTRACT, STEPHANIA TETRANDRA EXTRACT, WATER, YEAST BETA-GLUCAN, ZANTHOXYLUM BUNGEANUM FRUIT EXTRACT

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

LabelerGuangzhou Oupeng Cosmetics Co., Ltd.
FDA applicationM028 (OTC MONOGRAPH DRUG)
Labeler code85772
First marketedJul 2026
Product typeHuman Otc Drug
Portfolio8 products on file
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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 47 words ▾

Uses For the removal of common and plantar warts The common wart is easily recognized by the rough "cauliflower-like" appearance of the surface The plantar wart is recognized by its location only on the bottom of the foot, its tenderness, and the interruption of the footprint pattern

⏱️ Dosage and Administration 53 words ▾

Directions Wash the affected area and soak the wart in warm water for 5 minutes, then dry thoroughly. Apply a small amount of the solution to sufficiently cover each wart and let it dry completely. Repeat this procedure once or twice daily as needed (until wart is removed) for up to 12 weeks.

⚠️ Warnings 113 words ▾

Warnings For external use only. Do not use On irritated skin or on any area that is infected or reddened. On broken or recently shaven skin.

On moles, birthmarks, warts with hair growing from them, genital warts, or warts on the face or mucous membranes. When using this product Avoid contact with eyes. If contact occurs, rinse immediately with water.

Cap bottle tightly and store at room temperature away from heat. Stop use and ask a doctor if Redness or irritation develops. Discomfort persists.

If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 5 words ▾

Active ingredient Salicylic acid 17%

🧪 Inactive Ingredients 54 words ▾

Inactive ingredients 1,2-HEXANEDIOL, ALCOHOL, ALLANTOIN, ARGININE, BISABOLOL, BUTYLENE GLYCOL, CAPSICUM FRUTESCENS FRUIT EXTRACT, CYNANCHUM ATRATUM EXTRACT, ETHYLHEXYLGLYCERIN, GENTIANA SCABRA ROOT EXTRACT, GYNOSTEMMA PENTAPHYLLUM EXTRACT, HYALURONIC ACID, HYDROXYACETOPHENONE, MENTHYL LACTATE, PEG-40 HYDROGENATED CASTOR OIL, PHENOXYETHANOL, PIPER METHYSTICUM ROOT EXTRACT, PROPYLENE GLYCOL, SOPHORA ANGUSTIFOLIA ROOT EXTRACT, STEPHANIA TETRANDRA EXTRACT, WATER, YEAST BETA-GLUCAN, ZANTHOXYLUM BUNGEANUM FRUIT EXTRACT

🎯 Purpose 3 words ▾

Purpose Wart remover

📄 Do Not Use 40 words ▾

Do not use On irritated skin or on any area that is infected or reddened. On broken or recently shaven skin. On moles, birthmarks, warts with hair growing from them, genital warts, or warts on the face or mucous membranes.

📄 When Using This Product 26 words ▾

When using this product Avoid contact with eyes. If contact occurs, rinse immediately with water. Cap bottle tightly and store at room temperature away from heat.

📄 Stop Use and Ask a Doctor If 13 words ▾

Stop use and ask a doctor if Redness or irritation develops. Discomfort persists.

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant or breast-feeding, ask a health professional before use.

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Other Information 12 words ▾

Other information Store in a cool, dry place away from direct sunlight.

📄 Questions or Comments 6 words ▾

Questions or comments? 934-935-7135 / [email protected]

📄 Package Label / Principal Display Panel 32 words ▾

Ladoverna PRECISION WART CARE For Common & Plantar Warts 17% SALICYLIC ACID TARGET. PROTECT. REMOVE. PRECISE APPLICATOR PROTECTIVE WART STICKERS 28-DAY PROGRESS TRACKER FAST-DRYING FORMULA 1 FL. OZ. (30ml) PRECISION WART CARE

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 Guangzhou Oupeng Cosmetics Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangzhou Oupeng Cosmetics 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.
← 85772-0010-01 · Guangzhou 85773-0204-60 · YOALI →
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.