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ULTRA STRENGTH ZHENG GU SHUI MENTHOL AND CAMPHOR 4.1 g/100mL; 4.1 g/100mL Liniment

by GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD · 1 BOTTLE, WITH APPLICATOR in 1 BOX (59321-056-02) / 88 mL in 1 BOTTLE, WITH APPLICATOR
NDC 59321-0056-02
🏷️ FDA NDC (as labeled) 59321-056-02 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced 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

FDA NDC (as labeled) 59321-056-02
Product NDC 59321-056
11-digit billing NDC 59321005602
UNII 5TJD82A1ET, L7T10EIP3A
Application # M017
SPL Set ID 53397663-044d-4e48-989b-2c6257af5f84
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-04-04
Marketing end 2028-05-01
Route PERCUTANEOUS
Dosage form LINIMENT
Substance CAMPHOR (SYNTHETIC); MENTHOL
Why two NDCs? The FDA registers this code as 59321-056-02 — 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 → 59321-0056-02. 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.

🏭 Manufacturer & labeler

LabelerGUANGXI YULIN PHARMACEUTICAL GROUP CO LTD
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code59321
First marketedApr 2023
Product typeHuman Otc Drug
Portfolio2 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.

🩺 Clinical

🧪 What is this product?

Ultra Strength Zheng Gu Shui is a liniment (liquid preparation applied to skin) that contains menthol and synthetic camphor as active ingredients. Both of these ingredients are commonly used in topical products for their warming and cooling sensations, and they function as counterirritants that are typically applied to skin over muscles and joints. This is an over-the-counter monograph product, meaning it is marketed under FDA's established rules for this category of topical analgesic products rather than through an individual drug 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.

🧪 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 0MF1EI01KJ
    Angelica pubescens root is a plant-derived ingredient used as a flavoring agent and traditional botanical component in some herbal and natural formulations to enhance taste and provide characteristic aroma.
  • UNII 74U2K67MND
    A plant extract from Ardisia crenata root used as a natural ingredient in formulations. It may serve as a flavoring agent, colorant, or botanical additive in traditional or herbal medicine preparations.
  • UNII 0E347O3NMS
    A plant-derived ingredient from the roots of Ardisia gigantifolia. It functions as a flavoring agent and may help improve the taste or sensory qualities of the medicine.
  • UNII L1D54XX58F
    A plant-derived substance from the roots of Artocarpus styracifolius, a tropical tree. It may function as a natural binder or thickening agent to help hold the medicine's ingredients together or improve texture.
  • UNII M8FV4OUJ6F
    A plant-derived substance from calophyllum membranaceum tree. It may serve as a natural emollient, skin conditioning agent, or botanical extract in topical formulations to help soften and protect the skin.
  • UNII 8Z18N528CU
    A plant extract from clematis chinensis root used in traditional formulations. It may serve as a natural flavoring agent, colorant, or texture modifier in the medicine.
  • UNII P7PXC11S4S
    A plant extract from turmeric root used as a natural colorant and flavoring agent. It provides yellow-orange color and mild flavor to the medicine.
  • UNII BRM37UP34O
    A plant-derived ingredient from Cyathula officinalis root. It may be used as a binder or filler to help hold tablet ingredients together and add bulk to the formulation.
  • UNII CZP7EPR012
    A plant-derived ingredient from the root of Cynanchum paniculatum. It may function as a binder or thickening agent to help hold the medicine together or improve its consistency in the formulation.
  • UNII L878N1L0AR
    A plant extract from the bark of the eucommia tree, used in some formulations as a thickening or binding agent to help hold the medicine together and control how it dissolves.
  • UNII 81P4AE27JI
    Kadsura coccinea is a plant-derived ingredient used in traditional medicine formulations. It may function as a flavoring agent, natural colorant, or botanical extract to support the medicine's overall composition.
  • UNII U33KT97I2D
    A plant-derived substance from Lasiobema championii stems used as a natural binder or filler in formulations to help hold tablet or capsule ingredients together and add bulk to the medicine.
  • UNII 3WTU9E1VPU
    A plant extract from the root of Maclura cochinchinensis, a tree native to Southeast Asia. It may function as a natural colorant, flavoring agent, or botanical ingredient in formulations.
  • UNII TBW2M73EBN
    A plant-derived substance from millettia pulchra root. Used in formulations as a natural binding agent or texture modifier to help hold ingredients together and improve product consistency.
  • UNII 638OW484M3
    A plant-derived substance from the root bark of Periploca sepium. It may function as a natural binder or filler to help hold tablet ingredients together or add bulk to the formulation.
  • UNII AMU868N7QW
    A plant-derived ingredient from Piper hancei, used as a flavoring agent and potential sensory enhancer in medications to improve taste or aroma of the formulation.
  • UNII L3VA8YE43K
    A plant-derived ingredient from creeping pothos roots, used as a binder or thickening agent to help hold the medicine together and improve its texture or consistency.
  • UNII 7TRV45YZF7
    A plant extract from Japanese knotweed root used as a natural ingredient. It functions as an antioxidant and preservative to help maintain product stability and shelf life.
  • UNII 32E1WPH24S
    A plant extract from Sarcandra glabra, a traditional medicinal herb. It may be included in formulations for flavoring, coloring, or as a botanical additive to support the product's intended characteristics.
  • UNII 0SVU07NNEC
    A plant extract from the securidaca inappendiculata root used in traditional formulations. It may function as a binder or natural additive to help hold tablet ingredients together or improve product consistency.
  • UNII 66ZQ85S65H
    A plant-derived substance from the roots of Sparganium stoloniferum, used in some formulations as a natural binder or thickening agent to help hold ingredients together and give the medicine its solid form.
  • UNII N51VZ363BA
    A plant extract derived from the stem of Spatholobus suberectus, a tropical vine. It's used in herbal and traditional medicine formulations as a natural ingredient to support the product's therapeutic properties and stability.

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

The official label also statesInactive ingredients Alcohol, angelica dahurice root, angelica pubescens root, ardisia crenata root, ardisia gigantifolia root, artocarpus styracifolius root, calophyllum membranaceum whole, clematis chinensis root, curcuma phaeocaulis root, cyathulae officinalis root, cynanchum paniculatum root, eucommia ulmoides bark, kadsura coccinea whole, lasiobema championii stem, maclura cochinensis root, millettia pulchra root, periploca sepium root bark, piper hancei top, pothos repens root, reynoutria japonica root, sarcandra glabra top, securidaca inappendiculata root, spargnaium stoloniferum root, and spatholobus suberectus stem.

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.

💲 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Ultra Strength Zheng Gu Shui 4.1 g/100mL; 4.1 g/100mLthis 59321-0056-02 GUANGXI 1 bottle — — 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

🏛️
2023
On the market since
Apr 2023
📍
2026
Currently FDA-listed
3 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
59321-0056-02 You're viewing this 1 BOTTLE, WITH APPLICATOR in 1 BOX (59321-056-02) / 88 mL in 1 BOTTLE, WITH APPLICATOR 2023-04-04 Active

🧭 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 — Not published for this NDC No photo available yet for this listing.
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 FDA registers it as 59321-056-02, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 59321-0056-02, written without dashes as 59321005602. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 59321-0056-02, the first segment (59321) is the labeler code FDA assigned to GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD; the middle segment (0056) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page it is currently marketed — but GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD has reported a marketing end date of 2028-05-01, after which this package is expected to stop being marketed. The directory data on this page refreshes weekly.
Who lists this product with the FDA?
GUANGXI YULIN PHARMACEUTICAL GROUP 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.

📄 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 🤒 Adverse Reactions 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 27 words ▾

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

⏱️ Dosage and Administration 37 words ▾

Directions ■ Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. ■ Children under 2 years of age: do no use or consult a doctor.

⚠️ Warnings 5 words ▾

Warnings For external use only

🤒 Adverse Reactions 16 words ▾

Report any unexpected side effects from the use of this product to the FDA MedWatch Program.

📦 Storage and Handling 15 words ▾

Other information ■ store at room temperature, 20 to 25 C (68 to 77 F)

🧪 Active Ingredient 6 words ▾

Active ingredient Menthol 4.1% Camphor 4.1%

🧪 Inactive Ingredients 74 words ▾

Inactive ingredients Alcohol, angelica dahurice root, angelica pubescens root, ardisia crenata root, ardisia gigantifolia root, artocarpus styracifolius root, calophyllum membranaceum whole, clematis chinensis root, curcuma phaeocaulis root, cyathulae officinalis root, cynanchum paniculatum root, eucommia ulmoides bark, kadsura coccinea whole, lasiobema championii stem, maclura cochinensis root, millettia pulchra root, periploca sepium root bark, piper hancei top, pothos repens root, reynoutria japonica root, sarcandra glabra top, securidaca inappendiculata root, spargnaium stoloniferum root, and spatholobus suberectus stem.

🎯 Purpose 5 words ▾

Purpose External analgesic External analgesic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 59321-0055-01 · GUANGXI 59336-0001-01 · JW →
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.