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China-Gel Topical Pain Reliever Menthol and Camohor (synthetic) 50 mg/g; 30 mg/g Cream, 3628.7 g — NDC 76305-0300-06 package photo

China-Gel Topical Pain Reliever Menthol and Camohor (synthetic) 50 mg/g; 30 mg/g Cream, 3628.7 g

by China-Gel, LLC · 3628.7 g in 1 JUG (76305-300-06)
NDC 76305-0300-06
🏷️ FDA NDC (as labeled) 76305-300-06 billing pads the product segment with a zero
This package
Contains3628.7 g Pack sizes7 compare ↓
Also comes in: 56.8 g 76305-0300-13 113.5 g 76305-0300-02 170 g 76305-0300-03 226.8 g 76305-0300-04 453.6 g 76305-0300-05 199578.5 g 76305-0300-07
OTC On market Non-controlled
🗂️ Data synced Aug 27, 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) 76305-300-06
Product NDC 76305-300
11-digit billing NDC 76305030006
RxCUI 1312283, 1722364
UNII L7T10EIP3A, 5TJD82A1ET
UPC 0687806100167
Application # M017
SPL Set ID ba6c7e97-d740-484b-8711-55fa7ab15784
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2000-08-19
Route TOPICAL
Dosage form CREAM
Substance MENTHOL; CAMPHOR (SYNTHETIC)
Why two NDCs? The FDA registers this code as 76305-300-06 — 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 → 76305-0300-06. 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

LabelerChina-Gel, LLC
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code76305
First marketedAug 2000
Product typeHuman Otc Drug
Portfolio3 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?

China-Gel Topical Pain Reliever is a cream applied to the skin that contains menthol and synthetic camphor. Both ingredients are commonly used in over-the-counter topical products to produce a cooling or warming sensation and are typically included to help relieve minor muscle and joint discomfort. This product is marketed as an OTC monograph drug, meaning it follows established FDA guidelines for this category of pain-relief cream rather than being individually approved.

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 ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII DTN01M69SN
    A plant extract from angelica root used as a flavoring agent and fragrance component in medicines. It adds taste and aroma to make the product more pleasant to take.
  • UNII CUQ3A77YXI
    Panax ginseng root is a plant extract traditionally used in herbal preparations. In medications, it may serve as an active botanical ingredient or be included for flavoring and as a natural preservative or binder in formulations.
  • UNII 4Q93RCW27E
    A synthetic polymer made from acrylic acid that's crosslinked for stability. It acts as a thickener and gelling agent in creams and gels, helping the medicine spread evenly and maintain its texture.
  • UNII H3R47K3TBD
    FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
  • UNII I753WB2F1M
    FD&C Yellow No. 5 is a synthetic yellow colorant approved by the FDA. It is added to medicines to make pills, tablets, or liquids visually distinct and easier to identify.
  • UNII T07U1161SV
    A plant extract from witch hazel leaves, used in medicines as a natural astringent and skin-soothing agent. It helps reduce irritation and is often included in topical formulations for its mild anti-inflammatory properties.
  • UNII ND2M416302
    Isopropyl alcohol is a clear liquid solvent derived from petroleum. In medicines, it dissolves active ingredients and other components, helps the product flow smoothly, and aids in sterilization during manufacturing.
  • UNII 9RES347CKG
    A fragrant oil derived from lavandin plants, used as a flavoring and aromatic agent to improve the taste and smell of medicines.
  • UNII CAL22UVI4M
    A synthetic emulsifier derived from sorbitol and fatty acids. It helps mix oil and water-based ingredients together and improves the texture and stability of the medicine.
  • UNII 9O3K93S3TK
    Trolamine is an alkaline compound used as a pH buffer and emulsifier in medicines. It helps neutralize acids, stabilize formulations, and enable mixing of oil and water-based ingredients.
  • 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.

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

The official label also statesAloe Barbadensis Leaf Extract, Angelica Archangelica Root Extract, Blue 1, Carbomer, Hamarnelis Virginiana (Witch Hazel) Extract, Isopropyl Alcohol, Lavandula hybrida abrialis (Lavender) Oil, Panax Gingseng Root Extract, Polysorbate 60, Triethanolamine, Water, Yellow 5

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 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.
Try another pack size: 56.8 g 113.5 g 170 g 226.8 g 453.6 g 199578.5 g
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
China-Gel Topical Pain Reliever 50 mg/g; 30 mg/gthis 76305-0300-06 China-Gel, 3628.7 g — — FDA listed —
China-Gel Topical Pain Reliever 50 mg/g; 30 mg/g 76305-0301-02 China-Gel, 113.5 g — — FDA listed —
Aulief Topical Pain Reliever 30 mg/g; 50 mg/g 76305-0302-01 China-Gel, 90.7 g — — FDA listed —
China-Gel 50 mg/g; 30 mg/g 76305-0402-01 China-Gel, 113.5 g — — FDA listed —
Healthy Back Institute Rub On Relief .05 g/g; .03 g/g 79804-0618-03 Eagle 87.1 g — — FDA listed —
Healthy Back Institute Rub On Relief .03 g/g; .05 g/g 83084-0618-03 Fullstack 87.1 g — — FDA listed —
Core Relief 3 g/100mL; 5 g/100mL 87179-0053-02 Copper 59 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

🏛️
2000
On the market since
Aug 2000
📍
2026
Currently FDA-listed
26 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
76305-0300-02 113.5 g in 1 JAR (76305-300-02) 2000-08-19 Active
76305-0300-03 170 g in 1 TUBE (76305-300-03) 2000-08-19 Active
76305-0300-04 226.8 g in 1 JAR (76305-300-04) 2000-08-19 Active
76305-0300-05 453.6 g in 1 JAR (76305-300-05) 2000-08-19 Active
76305-0300-06 You're viewing this 3628.7 g in 1 JUG (76305-300-06) 2000-08-19 Active
76305-0300-07 199578.5 g in 1 DRUM (76305-300-07) 2000-08-19 Active
76305-0300-13 56.8 g in 1 TUBE (76305-300-13) 2000-08-19 Active

Pack size FAQ

What quantity is in NDC 76305-0300-06?
NDC 76305-0300-06 contains 3628.7 g — 3628.7 g in 1 jug.
What is the difference between NDC 76305-0300-06 and NDC 76305-0300-13?
Both are China-Gel Topical Pain Reliever Menthol and Camohor (synthetic) 50 mg/g; 30 mg/g Cream — the drug itself is identical. NDC 76305-0300-06 is the 3628.7 g package, while NDC 76305-0300-13 is the 56.8 g package.
What NDC number is used to bill for this package of China-Gel Topical Pain Reliever Menthol and Camohor (synthetic) 50 mg/g; 30 mg/g Cream?
Bill NDC 76305-0300-06 — the 11-digit billing format is 76305030006. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 76305-300-06, 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: 76305-0300-06, written without dashes as 76305030006. 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 76305-0300-06, the first segment (76305) is the labeler code FDA assigned to China-Gel, LLC; the middle segment (0300) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (06) 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: this package is listed as actively marketed, with no marketing end date reported by China-Gel, LLC. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 6 other package presentations of this same product, including 56.8 g (76305-0300-13), 113.5 g (76305-0300-02), 170 g (76305-0300-03). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
China-Gel, LLC 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 26 words ▾

Uses Temporary relief from minor aches and pains of sore muscles and joints associated with: arthritis bursitis simple backaches sports injuries strains of muscle and joint

⏱️ Dosage and Administration 32 words ▾

Directions Adults or children 2 years of age or older Cleanse area - apply liberally over affected area as needed Massage into skin until absorbed Repeat up to 4 times a day

⚠️ Warnings 12 words ▾

Warnings For external use only avoid contact with eyes and mucous membranes

📦 Storage and Handling 25 words ▾

Other information Store in a cool, dry place Minor separation may occur Keep closed when not in use Do not puncture or incinerate this packaging

🧪 Active Ingredient 6 words ▾

Active Ingredients Camphor 3.00% Menthol 5.00%

🧪 Inactive Ingredients 35 words ▾

Inactive Ingredients Aloe Barbadensis Leaf Extract, Angelica Archangelica Root Extract, Blue 1, Carbomer, Hamarnelis Virginiana (Witch Hazel) Extract, Isopropyl Alcohol, Lavandula hybrida abrialis (Lavender) Oil, Panax Gingseng Root Extract, Polysorbate 60, Triethanolamine, Water, Yellow 5

🎯 Purpose 5 words ▾

Purpose Topical Analgesic Topical Analgesic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 76297-0009-01 · LABORATORIOS 76305-0301-02 · China-Gel, →
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.