Home › NDC Lookup › Ingredients › Methyl Salicylate › 57598-0111-01
Koong Yick Hung Fa Methyl Salicylate 25 g/100mL Oil — NDC 57598-0111-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Koong Yick Hung Fa Methyl Salicylate 25 g/100mL Oil — NDC 57598-111-01 (Billing 57598-0111-01)

by Ling Nam Medicine Factory (H.K.) Ltd. · 1 BOTTLE in 1 BOX / 60 mL in 1 BOTTLE

This is a package of Koong Yick Hung Fa Methyl Salicylate 25 g/100mL Oil from Ling Nam Medicine Factory (H.K.) Ltd., marketed since Feb 2021 and currently FDA-listed. It is this product's only package size.

NDC 57598-0111-01
🏷️ FDA NDC (as labeled) 57598-111-01 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 57598-111-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
57598 labeler · 111 product · 01 package
Package marketed since
Feb 4, 2021
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
4892758020609
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 57598-111-01
Product NDC 57598-111
11-digit billing NDC 57598011101
RxCUI 2468738
UNII LAV5U5022Y
UPC 4892758020609
Application # M017
SPL Set ID 9c8a121d-6da2-4435-a2d7-a0b71d10740d
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-02-04
Route TOPICAL
Dosage form OIL
Substance METHYL SALICYLATE
Quick answers
  • RxCUI (RxNorm): 2468738
Why two NDCs? The FDA registers this code as 57598-111-01 — 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 → 57598-0111-01. 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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • It's a topical pain reliever — you apply it right to the skin where it hurts. It's used for temporary relief of minor aches and pains in your muscles and joints, things like arthri...
  • What is methyl salicylate actually used for?
  • No — and this is really important. You should never use methyl salicylate products with a heating pad, and avoid applying them when you're sweating from exercise or heat. Heat caus...
  • Is it safe to use under a heating pad or wrap?
📖 Read our full Methyl Salicylate guide →

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 eachPer 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
57598-0111-01 You're viewing this Main listing 1 BOTTLE in 1 BOX / 60 mL in 1 BOTTLE 2021-02-04 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Koong Yick Hung Fa 25 g/100mLthis 57598-0111-01 Ling 1 bottle — — FDA listed —
Ling Nam Hung Far 25 g/100mL 57598-0112-01 Ling 1 bottle — — FDA listed —
AVON Foot Works Arthritis Achy Foot and Muscle 25 g/100mL 68577-0257-00 COSMAX 1 tube — — 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

🏛️
2021
On the market since
Feb 2021
📍
2026
Currently FDA-listed
5 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.

🧪 Avoiding an ingredient? See Methyl Salicylate inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

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

  • UNII A4WO0626T5
    A natural aromatic oil extracted from cinnamon bark, used as a flavoring agent to improve taste and add spice notes to medicines.
  • UNII S92U8SQ71V
    A natural oil extracted from cinnamon leaves used as a flavoring agent and fragrance in medicines. It provides taste and aroma to make the product more pleasant to take.
  • UNII 578389D6D0
    Clove oil is an essential oil derived from clove plant buds. It's used in medicines as a flavoring agent and for its mild preservative properties to help maintain product stability.
  • UNII Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • UNII 4QP5U84YF7
    A synthetic green colorant used to tint medicines and make them visually distinctive. It helps identify the medication and may improve appearance of tablets or capsules.
  • UNII ND733RX3JN
    A synthetic red colorant used to give medicines their color. It helps identify the medication and makes it visually distinguishable from other drugs.
  • UNII 350KA7O6HK
    D&C Violet No. 2 is a synthetic purple dye approved by the FDA for use in medicines. It serves as a colorant to make tablets, capsules, or liquids visually distinct for identification purposes.
  • UNII 44F3HYL954
    A synthetic yellow dye used to color medicines and supplements. It helps make tablets and capsules visually distinctive for identification and product branding purposes.
  • UNII N6K5787QVP
    Light mineral oil is a clear, odorless liquid derived from petroleum. In medicines, it acts as a lubricant and emollient to help the product spread smoothly and improve texture.

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

The official label also statesChinese cinnamon oil, Cinnamon leaf oil, Clove oil, Coconut oil, D&C Green No.6, D&C Red No.17, D&C Violet No.2, D&C Yellow No.11, Light mineral oil

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

LabelerLing Nam Medicine Factory (H.K.) Ltd.
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code57598
First marketedFeb 2021
Product typeHuman Otc Drug
Portfolio5 products on file

More NDCs from Ling Nam Medicine Factory (H.K.) Ltd. labeler code 57598

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 📄 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 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 21 words ▾

Uses For temporary relief of minor aches and pains of muscles and joints due to: arthritis strains bruises sprains simple backache

⏱️ Dosage and Administration 43 words ▾

Directions Adults and children 12 years of age and older: Apply not more than 3 to 4 drops to the affected area not more than 3 to 4 times daily. Children under 12 years of age: Do not use or consult a doctor.

⚠️ Warnings 154 words ▾

Warnings For external use only Do not use on wounds irritated or damaged skin sensitive skin with a heating pad with, or at the same time as, other external analgesic products if allergic to aspirin or salicylates if allergic to any ingredients of this product if pregnant When using this product avoid contact with the eyes or on mucous membranes do not bandage tightly do not apply to wounds or damaged skin do not use 1 hour before or after bathing Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days symptoms clear up and occur again within a few days excessive irritation of the skin develops redness is present If pregnant, ask health professional before use.

Keep out of reach of children to avoid accidental poisoning . If swallowed, get medical help or contact a Poison Control Center right away. Do not use otherwise than as directed.

📦 Storage and Handling 12 words ▾

Other information Store in a cool place Close tightly after each use

🧪 Active Ingredient 8 words ▾

Active Ingredients Purpose Methyl salicylate 25% External analgesic

🧪 Inactive Ingredients 27 words ▾

Inactive ingredients Chinese cinnamon oil, Cinnamon leaf oil, Clove oil, Coconut oil, D&C Green No.6, D&C Red No.17, D&C Violet No.2, D&C Yellow No.11, Light mineral oil

🎯 Purpose 8 words ▾

Active Ingredients Purpose Methyl salicylate 25% External analgesic

📄 Do Not Use 42 words ▾

Do not use on wounds irritated or damaged skin sensitive skin with a heating pad with, or at the same time as, other external analgesic products if allergic to aspirin or salicylates if allergic to any ingredients of this product if pregnant

📄 When Using This Product 34 words ▾

When using this product avoid contact with the eyes or on mucous membranes do not bandage tightly do not apply to wounds or damaged skin do not use 1 hour before or after bathing

📄 Stop Use and Ask a Doctor If 35 words ▾

Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days symptoms clear up and occur again within a few days excessive irritation of the skin develops redness is present

🤰 If Pregnant or Breast-Feeding 7 words ▾

If pregnant, ask health professional before use.

📄 Keep Out of Reach of Children 31 words ▾

Keep out of reach of children to avoid accidental poisoning . If swallowed, get medical help or contact a Poison Control Center right away. Do not use otherwise than as directed.

📄 Questions or Comments 18 words ▾

Questions? +1-888-915-6789 M-F 9am to 5pm Pacific Time. You may report serious side effects to this phone number.

📄 Package Label / Principal Display Panel 38 words ▾

PRINCIPAL DISPLAY PANEL - 60 ml Bottle Box NDC No. : 57598-111-01 KOONG YICK & COMPANY LIMITED KOONG YICK KOONG YICK HUNG FA OIL EXTERNAL ANALGESIC 2 FI. Oz. (60ml) PRINCIPAL DISPLAY PANEL - 60 ml Bottle Box

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 Ling Nam Medicine Factory (H.K.) Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Ling Nam Medicine Factory (H.K.) 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.
← 57597-0043-01 · Wong 57598-0112-01 · Ling →
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.