Home › NDC Lookup › Ingredients › Menthol › 68007-0403-01
Zhuifeng Gao Pain Relieving Menthol 35 mg Plaster — NDC 68007-0403-01 package photo

Zhuifeng Gao Pain Relieving Menthol 35 mg Plaster

by GUILIN CHINA RESOURCES TIANHE PHARMACEUTICAL CO LTD · 2 POUCH in 1 BOX (68007-403-01) / 5 PLASTER in 1 POUCH
NDC 68007-0403-01
🏷️ FDA NDC (as labeled) 68007-403-01 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

⚠️
Other active recalls for Menthol (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Mar 20, 2026 — This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality. (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.) · FDA recall D-0458-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 68007-403-01
Product NDC 68007-403
11-digit billing NDC 68007040301
RxCUI 2566787
UNII L7T10EIP3A
Application # M017
SPL Set ID 3f12da60-26d1-4407-8e02-c3213ea3ad2a
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-06-26
Marketing end 2028-10-31
Route TRANSDERMAL
Dosage form PLASTER
Substance MENTHOL
Why two NDCs? The FDA registers this code as 68007-403-01 — 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 → 68007-0403-01. 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.

🏭 Manufacturer & labeler

LabelerGUILIN CHINA RESOURCES TIANHE PHARMACEUTICAL CO LTD
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code68007
First marketedJun 2022
Product typeHuman Otc Drug
Portfolio4 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

📗 Our plain-language guide HelloPharmacist
  • Menthol is found in a lot of over-the-counter topical products — creams, gels, patches, sprays, and powders. Depending on the product, it's used to temporarily ease minor muscle an...
  • Start with clean, dry skin — free of lotions or creams — before applying the patch. Peel the backing off and press the sticky side firmly to the sore area. Most menthol patches sho...
  • Yes, a mild burning or tingling feeling right after applying a menthol product is common and usually settles down within a few days of regular use. What's not normal is severe burn...
  • Is that burning sensation after I apply it normal?
📖 Read our full Menthol 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.

🧪 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 5QIU26R6P1
    Achyranthes bidentata root is a plant-derived ingredient used in traditional formulations. It typically functions as a binder or filler to help hold tablet components together and add bulk to the dosage form.
  • 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 B66F4574UG
    A plant-derived ingredient from Chinese angelica root, used as a natural flavoring and fragrance agent in medicines. It may also serve as a traditional ingredient to support formulation stability.
  • UNII 086263LQDD
    A natural extract from sappan wood, a tropical tree. Used as a colorant to give medicines their red or brown appearance.
  • UNII WS4CQ062KM
    A plant-derived spice from cinnamon bark, used as a flavoring agent to mask bitter tastes and add pleasant aroma to medicines.
  • UNII E5GY4I6YCZ
    A fragrant liquid extracted from cinnamon bark, used as a flavoring agent to improve the taste of medicines and make them more pleasant to take.
  • 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 LB1GQP4253
    A plant extract from the teasel root used as a traditional herbal ingredient. In medicines, it may function as a filler or binder to help hold the product together and maintain its form.
  • UNII M3YJ2C28IC
    Dragon's blood is a natural red resin obtained from tropical plants. It's used in medicines as a colorant and binding agent to give pills and capsules their appearance and help hold ingredients together.
  • UNII R9XLF1R1WM
    Frankincense is a natural resin from the Boswellia tree. It's used in medicines as a binder or thickener to help hold ingredients together and improve the product's consistency and texture.
  • UNII 0A62964IBU
    Isoprene is a light, volatile liquid hydrocarbon derived from petroleum or natural sources. In medicines, it may be used as a solvent or carrier to help dissolve or distribute active ingredients evenly throughout a formulation.
  • UNII LR7SZ0O0B9
    A plant-derived substance from Knoxia roxburghii roots, used in traditional medicine formulations. It may serve as a natural binder or filler to help hold tablet ingredients together and give the medicine its shape.
  • UNII 7EV65EAW6H
    Lanolin is a waxy substance derived from sheep's wool. It's used in medicines as an emollient and skin-conditioning agent to soften formulations and improve spreadability in topical products like creams and ointments.
  • UNII 42LD90786Y
    Lesser galangal root is a plant-derived ingredient used as a flavoring agent and traditional ingredient in some herbal or botanical formulations. It may contribute taste and aroma to the medicine.
  • UNII 517Q7XRT2T
    A plant-derived ingredient from the root of Lindera aggregata. It may be used as a natural flavoring agent, fragrance component, or traditional botanical extract in formulations.
  • UNII T5L8T28FGP
    Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
  • UNII JC71GJ1F3L
    Myrrh is a natural resin obtained from a tree, traditionally used in medicines and perfumes. It may serve as a flavoring agent, fragrance, or mild preservative in formulations.
  • UNII 2LQ0UUW8IN
    A natural rubber material derived from the rubber tree. It's used as a coating or component in capsule shells and drug delivery devices to provide structure, flexibility, and controlled release of the medication.
  • UNII 5Z2WW4J6RI
    A plant root extract used in traditional herbal formulations. It may function as an active botanical ingredient or flavoring agent, though in many modern medicines it serves primarily to support the product's traditional composition and stability.
  • UNII 7V3N80T4VS
    Ocimum gratissimum is a plant commonly known as African basil. It's used in formulations as a flavoring agent and may provide antimicrobial properties to help preserve the product.
  • UNII VX6GD6M93V
    A plant-derived substance from peony root used as a natural colorant, flavoring agent, or traditional ingredient in some formulations. It may help create the product's appearance or taste profile.
  • UNII X72Z47861V
    Paprika is a red spice powder made from dried peppers. It's used in medicines as a colorant to give tablets or capsules a red or orange appearance.
  • 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 4T6H12BN9U
    Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
  • UNII 80IOP41EL7
    A plant-derived ingredient from the stem of Piper kadsura vine, used in traditional medicine formulations. It may function as a flavoring agent, natural extract, or botanical component to support the product's intended formulation.
  • UNII V9C81470RR
    A plant-derived ingredient from peach seeds used as a natural emollient and skin-conditioning agent in topical formulations. It helps soften and smooth the product's texture.
  • UNII 88S87KL877
    Rosin is a sticky resin extracted from pine trees. It's used in medicines as a binder and adhesive to help hold tablet ingredients together and improve how the medicine sticks to surfaces.
  • UNII 4VBL71TY4Y
    Safflower is a plant-derived ingredient used as a natural colorant and flavoring agent in medicines. It may also serve as a filler to add bulk to the formulation.
  • UNII 44LJ2U959V
    Styrene is a liquid synthetic chemical used as a solvent and plasticizer in some pharmaceutical coatings and film formulations. It helps dissolve active ingredients and creates flexible protective layers around tablets or capsules.
  • UNII SOI2LOH54Z
    Zinc oxide is a white mineral powder used in medicines as a protective barrier agent and color additive. It helps shield skin in topical products and may also serve as a filler or opacifying ingredient.

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

The official label also statesInactive ingredients achyranthes root, angelica sinensis root, basil oil, cassia bark, Chinese clematis root and rhizome, Chinese peony root with bark, cinnamon oil, dragon’s blood resin, fragrant angelica root, frankincense oleo-gum-resin, kadsura pepper stem, knoxia root, lanolin, lesser galangal rhizome, lindera root, mineral oil, myrrh oleo-gum-resin, notopterygium rhizome and root, paprika, periplocae cortex, persicae semen, petrolatum, pubescent angelica root, rosin, rubber, safflower, sappanwood heartwood, sichuan teasel root, styrene-isoprene, and zinc oxide on a cotton pad and covered with a protective paper film.

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
Gutong Tiegao Pain Relieving 35 mg 68007-0400-01 GUILIN 2 pouches — — FDA listed —
Zhuanggu Gao Pain Relieving 35 mg 68007-0402-01 GUILIN 2 pouches — — FDA listed —
Zhuifeng Gao Pain Relieving 35 mgthis 68007-0403-01 GUILIN 2 pouches — — 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

🏛️
2022
On the market since
Jun 2022
📍
2026
Currently FDA-listed
4 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
68007-0403-01 You're viewing this 2 POUCH in 1 BOX (68007-403-01) / 5 PLASTER in 1 POUCH 2021-05-11 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 ✓ 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 FDA registers it as 68007-403-01, 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: 68007-0403-01, written without dashes as 68007040301. 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 68007-0403-01, the first segment (68007) is the labeler code FDA assigned to GUILIN CHINA RESOURCES TIANHE PHARMACEUTICAL CO LTD; the middle segment (0403) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 GUILIN CHINA RESOURCES TIANHE PHARMACEUTICAL CO LTD has reported a marketing end date of 2028-10-31, 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?
GUILIN CHINA RESOURCES TIANHE PHARMACEUTICAL 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 📦 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: ■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains

⏱️ Dosage and Administration 40 words ▾

Directions ■ adults and children 2 years of age and older: remove the protective film from the plaster. Apply to affected area not more than 3 to 4 times daily. ■ children under 2 years of age: consult your physician.

⚠️ Warnings 18 words ▾

Warnings For external use only Allergy alert: This product contains natural rubber latex which may cause allergic reactions.

📦 Storage and Handling 29 words ▾

Other information ■ keep plasters tightly closed in the zip-lock pouch ■ store at 15 to 30 C (59 to 86 F) in a dry place away from sunlight

🧪 Active Ingredient 4 words ▾

Active Ingredients Menthol 3.5%

🧪 Inactive Ingredients 82 words ▾

Inactive ingredients achyranthes root, angelica sinensis root, basil oil, cassia bark, Chinese clematis root and rhizome, Chinese peony root with bark, cinnamon oil, dragon’s blood resin, fragrant angelica root, frankincense oleo-gum-resin, kadsura pepper stem, knoxia root, lanolin, lesser galangal rhizome, lindera root, mineral oil, myrrh oleo-gum-resin, notopterygium rhizome and root, paprika, periplocae cortex, persicae semen, petrolatum, pubescent angelica root, rosin, rubber, safflower, sappanwood heartwood, sichuan teasel root, styrene-isoprene, and zinc oxide on a cotton pad and covered with a protective paper film.

🎯 Purpose 3 words ▾

Purpose External Analgesic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 68007-0402-01 · GUILIN 68012-0002-13 · Santarus, →
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.