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HempNesic Menthol, Camphor 3.5 g/100mL; .2 g/100mL Gel, 236.58 mL — NDC 63347-0223-08 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

HempNesic Menthol, Camphor 3.5 g/100mL; .2 g/100mL Gel, 236.58 mL — NDC 63347-223-08 (Billing 63347-0223-08)

by Blaine Labs Inc. · 236.58 mL in 1 TUBE

This is a package of 236.58 mL of HempNesic Menthol, Camphor 3.5 g/100mL; .2 g/100mL Gel from Blaine Labs Inc., marketed since Apr 2018 and currently FDA-listed.

NDC 63347-0223-08
🏷️ FDA NDC (as labeled) 63347-223-08 billing pads the product segment with a zero
This package
Contains236.58 mL Pack sizes2 compare ↓
Product page 63347-0223-01 Also comes in: 88.7 ml 63347-223-01
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 3, 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 63347-223-08 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
63347 labeler · 223 product · 08 package
Package marketed since
Apr 1, 2018
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6334722308 3
FDA record last changed
Oct 3, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 63347-223-08
Product NDC 63347-223
11-digit billing NDC 63347022308
UNII L7T10EIP3A, 5TJD82A1ET
Application # M012
SPL Set ID 0239ada0-644d-4ef4-a3b8-df70246a3bc2
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2018-04-01
Route TOPICAL
Dosage form GEL
Substance MENTHOL; CAMPHOR (SYNTHETIC)
Why two NDCs? The FDA registers this code as 63347-223-08 — 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 → 63347-0223-08. 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

🧪 What is this product?

HempNesic Menthol, Camphor is a topical gel containing menthol and synthetic camphor. This product is an over-the-counter monograph drug, meaning it follows FDA's established rules for its category rather than undergoing individual product review. Menthol and camphor are commonly used in topical products for their cooling and warming sensations on the skin. These ingredients are typically applied to the skin surface to produce local effects in over-the-counter pain relief and personal care products.

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 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: 88.7 ml
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
63347-0223-01 63347-223-01 Main listing 88.7 mL in 1 TUBE 2018-04-01 — Active
63347-0223-08 You're viewing this 236.58 mL in 1 TUBE 2018-04-01 — Active

Pack size FAQ

What quantity is in this package?
This package contains 236.58 mL — 236.58 ml in 1 tube.
How does this package differ from NDC 63347-0223-01?
Both are HempNesic Menthol, Camphor 3.5 g/100mL; .2 g/100mL Gel — the drug itself is identical. This page's package is the 236.58 mL one, while NDC 63347-0223-01 is the 88.7 ml package.
What NDC number is used to bill for this package of HempNesic Menthol, Camphor 3.5 g/100mL; .2 g/100mL Gel?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
HempNesic 3.5 g/100mL; .2 g/100mLthis 63347-0223-08 Blaine 236.58 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

🏛️
2018
On the market since
Apr 2018
📍
2026
Currently FDA-listed
8 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.

💡 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 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 OZ0E5Y15PZ
    A plant extract from arnica flowers, used as a flavoring agent or fragrance component in medicines. It may also provide mild soothing properties to certain topical formulations.
  • UNII 19GBJ60SN5
    A naturally derived compound from cannabis plants used as an active pharmaceutical ingredient in certain FDA-approved medications. It is included to deliver the therapeutic substance rather than serve a traditional formulation role like binding or flavoring.
  • UNII 69VJ1LPN1S
    Cannabis sativa seed oil is a plant-based oil derived from hemp seeds. It's used in medicines as a carrier or emollient to help deliver active ingredients and improve product texture and absorption.
  • UNII NV1779205D
    A fatty alcohol derived from coconut oil or synthetic sources. It acts as a solvent, preservative, and antimicrobial agent to help dissolve ingredients and extend shelf life in liquid formulations.
  • UNII 809Y72KV36
    A synthetic polymer made from acrylic acid and crosslinked with allyl pentaerythritol. It's used as a thickening agent and gelling ingredient in creams, gels, and lotions to create the proper texture and help the medicine spread and stay on the skin.
  • UNII T7SWE4S2TT
    Cetyl hydroxyethylcellulose is a thickening agent and film-former made by modifying plant cellulose. It's used in topical medicines to increase texture, improve spreadability, and help create a protective barrier on skin.
  • 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.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • UNII UDA30A2JJY
    A plant extract from witch hazel used as an astringent and skin-conditioning agent in topical formulations. It helps tone and soothe the skin while functioning as a natural preservative.
  • UNII KEH0A3F75J
    Hexylene glycol is a clear liquid alcohol used as a solvent and preservative in medicines. It helps dissolve other ingredients and keeps the product stable during storage.
  • 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 AV092KU4JH
    A natural oil extracted from peppermint plants. It's used as a flavoring agent to mask bitter tastes and add a refreshing mint flavor to medicines, making them easier to take.
  • 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.
  • 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.
  • UNII C3M81465G5
    Spearmint oil is a natural flavoring extract from spearmint plants. It's added to medicines to improve taste and mask bitter flavors, making medications easier to take.
  • UNII VIF565UC2G
    Tea tree oil is an essential oil extracted from the leaves of the Australian tea tree plant. In medicines, it typically serves as a flavoring agent, fragrance, or antimicrobial component in topical formulations.
  • 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.

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

The official label also statesEthyl Alcohol Denatured, D.I. Water, Glycerin, Propylene Glycol, Cannabis Sativa Seed Oil (Hemp Seed Oil), Cannabidiol (CBD), Arnica Montana Flower Extract (Arnica Oil), Mentha Piperita (Peppermint) Oil, Hydroxyethylcellulose, Carbomer, triethanolamine, Mentha Viridis (Spearmint) Leaf Oil, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract, Hamamelis Virginiana (Witch Hazel) Extract, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Capsicum Annuum Fruit Extract, Phenoxyethanol, Caprylyl Alcohol, Ethylhexyl Glycerin, Hexylene Glycol

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

LabelerBlaine Labs Inc.
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code63347
First marketedApr 2018
Product typeHuman Otc Drug
Portfolio14 products on file

More NDCs from Blaine Labs Inc. labeler code 63347

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 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 25 words ▾

Uses For temporary relief from minor aches and pains of sore muscles and joints asociated with: • arthritis pain • backache • strains • sprains

⏱️ Dosage and Administration 27 words ▾

Directions: Use only as directed. Rub a thin film over the affected areas not more than four (4) times daily. Rinse hands after use with cool water.

⚠️ Warnings 5 words ▾

Warnings: For external use only.

🧪 Active Ingredient 8 words ▾

DRUG FACTS Active Ingredients: Menthol 3.5% Camphor 0.2%

🧪 Inactive Ingredients 67 words ▾

Inactive Ingredients Ethyl Alcohol Denatured, D.I. Water, Glycerin, Propylene Glycol, Cannabis Sativa Seed Oil (Hemp Seed Oil), Cannabidiol (CBD), Arnica Montana Flower Extract (Arnica Oil), Mentha Piperita (Peppermint) Oil, Hydroxyethylcellulose, Carbomer, triethanolamine, Mentha Viridis (Spearmint) Leaf Oil, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract, Hamamelis Virginiana (Witch Hazel) Extract, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Capsicum Annuum Fruit Extract, Phenoxyethanol, Caprylyl Alcohol, Ethylhexyl Glycerin, Hexylene Glycol

🎯 Purpose 3 words ▾

Purpose Topical Analgesic

📄 Ask a Doctor Before Use If 10 words ▾

Ask a doctor before use if you have: Sensitive skin

📄 When Using This Product 52 words ▾

When using this product: • Avoid contact with the eyes and/or mucous membranes • Do not use with other sprays, ointments, creams or liniments • Do not apply to irritated skin, & discontinue use if excessive skin irritation develops • Do not bandage • Do not use with heating pads or device

📄 Stop Use and Ask a Doctor If 24 words ▾

Stop use and contact your physician if: conditions worsen, or if symptoms persist for more than seven (7) days, or clear up and reoccur.

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant or breast-feeding: Ask a health professional before use

📄 Keep Out of Reach of Children 18 words ▾

Keep Out Of Reach Of Children: If swallowed, get medical help or contact a poison control center immediately.

📄 Other Information 29 words ▾

Flammable: Keep away from excessive heat or open flame.

Children under 2 years of age: Consult physician

Other Information: Store in a cool, dry place with lid closed tightly.

📄 Package Label / Principal Display Panel ~2 min read ▾

HempNesic ® PAIN-RELIEVING GEL NDC 63347-223-01 BLAINE LABS ® HempNesic ® PAIN-RELIEVING GEL MENTHOL AND CAMPHOR IN A GEL CONTAINING CAPSAICIN & HEMP OIL

3.0OZ (88.7 mL) DRUG FACTS Active Ingredients Purpose Menthol 3.5% ................................Topical Analgesic Camphor 0.2% ..............................Topical Analgesic Uses: For temporary relief from minor aches and pains of sore muscles and joints asociated with: • arthritis pain • backache • strains • sprains Warnings : For external use only. Flammable : Keep away from excessive heat or open flame. Ask a doctor before use if you have: Sensitive skin When using this product: • Avoid contact with the eyes and/or mucous membranes • Do not use with other sprays, ointments, creams or liniments • Do not apply to irritated skin, & discontinue use if excessive skin irritation develops • Do not bandage • Do not use with heating pads or device Stop use and contact your physician if: conditions worsen, or if symptoms persist for more than seven (7) days, or clear up and reoccur.

If pregnant or breast-feeding: Ask a health professional before use Children under 2 years of age: Consult physician Keep Out Of Reach Of Children: If swallowed, get medical help or contact a poison control center immediately. Directions: Use only as directed. Rub a thin film over the affected areas not more than four (4) times daily.

Rinse hands after use with cool water. Other Information: Store in a cool, dry place with lid closed tightly. Inactive Ingredients: Ethyl Alcohol Denatured, D.I.

Water, Glycerin, Propylene Glycol, Cannabis Sativa Seed Oil (Hemp Seed Oil ), Cannabidiol (Cbd), Arnica Montana Flower Extract (Arnica Oil), Mentha Piperita (Peppermint) Oil, Hydroxyethylcellulose, Carbomer, Triethanolamine, Mentha Viridis (Spearmint) Leaf Oil, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract, Hamamelis Virginiana (Witch Hazel) Extract, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Capsicum Annuum Fruit Extract, Phenoxyethanol, Caprylyl Alcohol, Ethylhexyl Glycerin, Hexylene Glycol Manufactured By: Blaine Labs, Inc.

11037 Lockport Place, Santa Fe Springs, CA 90670 Questions or Comments? Call (800) 307-8818 M-F 8am - 5pm (PST) *MADE IN THE USA Hempnesic_223_01.jpg Hempnesic_223_01

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Menthol, Camphor — the ingredient across all brands.

Top reported reactions

Application Site Burn2
Application Site Vesicles2
Blister2
Chemical Injury2
Drug Reaction With Eosinophilia And Systemic Symptoms2
Tubulointerstitial Nephritis2
Application Site Infection1

Age at onset

Adult1
Elderly3

Reporter sex

20 reports
Male · 35%
Female · 65%

Serious outcomes

Hospitalization5
Life-threatening1
Reports over time (by year) — tap or hover for the count & year
2023 2024 2025 2026 5 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

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 Blaine Labs Inc.. 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 1 other package presentation of this same product, including 88.7 ml (63347-0223-01). 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?
Blaine Labs Inc. 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.
← 63347-0130-01 · Blaine 63347-0380-01 · Blaine →
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.