Home › NDC Lookup › Ingredients › Menthol, Methyl Salicylate, Camphor › 87917-0001-02
Blaster Pain Relief Stick Menthol, Methyl Salicylate, Camphor 14 g/100g; 4 g/100g; 4 g/100g Stick — NDC 87917-0001-02 package photo

Blaster Pain Relief Stick Menthol, Methyl Salicylate, Camphor 14 g/100g; 4 g/100g; 4 g/100g Stick

by Kalahari Rose, LLC · 1 TUBE in 1 BOX (87917-001-02) / 15 g in 1 TUBE (87917-001-01)
NDC 87917-0001-02
🏷️ FDA NDC (as labeled) 87917-001-02 billing pads the product segment with a zero
This package
Contains15 g in 1 tube Pack sizes2 compare ↓
Also comes in: 30 g 87917-0001-04
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) 87917-001-02
Product NDC 87917-001
11-digit billing NDC 87917000102
RxCUI 2749412
UNII LAV5U5022Y, L7T10EIP3A, 5TJD82A1ET
UPC 0860011310754
Application # M017
SPL Set ID 587d660a-5f80-de5a-e063-6394a90aa287
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-08-07
Route TOPICAL
Dosage form STICK
Substance METHYL SALICYLATE; MENTHOL; CAMPHOR (SYNTHETIC)
Why two NDCs? The FDA registers this code as 87917-001-02 — 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 → 87917-0001-02. 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

LabelerKalahari Rose, LLC
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code87917
First marketedAug 2026
Product typeHuman Otc Drug
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?

Blaster Pain Relief Stick is a topical over-the-counter product marketed under FDA monograph rules. It contains methyl salicylate, menthol, and camphor, which are commonly used as counterirritants in pain relief products applied directly to the skin. These ingredients are typically included to produce a warming or cooling sensation that may help ease discomfort in muscles and joints. This product is meant for external use only on the skin surface.

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 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.
  • UNII J3TO6BUQ37
    Cajuput oil is a fragrant essential oil extracted from the cajuput tree. It's used in medicines as a flavoring agent and to add aroma, and may help mask unpleasant tastes.
  • 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 6KGS8SP16U
    A natural essential oil from turmeric root that gives medicines a yellow color and mild spice flavor. It's used mainly as a colorant and flavoring agent in tablets, capsules, and liquid formulations.
  • UNII U510PCG35P
    A plant-derived substance from Cyperus scariosus root, used in formulations as a natural binder or filler to help hold ingredients together and give the medicine its solid form.
  • UNII 2R04ONI662
    Eucalyptus oil is a fragrant liquid extracted from eucalyptus tree leaves. It's used in medicines as a flavor, scent, or soothing agent in topical products and cough preparations.
  • 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 211UF7M8N1
    A natural essential oil extracted from galbanum plant resin, used as a fragrance and flavoring ingredient to mask unpleasant tastes or odors in medicines.
  • UNII YC79BB3F4Y
    A plant-derived oil from hibiscus seeds used in medicines as an emollient and skin-conditioning agent. It helps soften and smooth the product's texture, often in topical formulations.
  • UNII XK4IUX8MNB
    Hypericum perforatum, also known as St. John's Wort, is a plant extract used in some medicines. It may serve as an active botanical ingredient or flavoring agent depending on the formulation.
  • UNII R09L2486DI
    A plant-derived ingredient from Kunzea ambigua, a shrub native to Australia. It may function as a natural flavoring agent, fragrance component, or botanical extract in the formulation.
  • 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 K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • UNII V038D626IF
    A plant extract from Withania somnifera root, traditionally used in herbal preparations. It may function as an active botanical ingredient or filler in formulations, though its primary role depends on the specific product formulation.

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

The official label also statesInactive Ingredients Beeswax (Cera Alba), Butyrospermum Parkii (Shea) Butter, Cinnamomum Cassia Oil, Curcuma Longa (Turmeric) Root Oil, Cyprus Scariosus Root Oil, Eucalyptus Globulus Leaf Oil, Eugenia Caryophyllus (Clove) Bud Oil, Ferula Galbaniflua (Galbanum) Resin Oil, Hibuscus Abelmoschus Seed Oil, Hypericum Perforatum Oil, Kunzea Ambigua Branch/Leaf/Twig Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Melaleuca Leucadendron Cajaputi Oil, Withania Somnifera Root Extract.

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.
Try another pack size: 30 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
Blaster Pain Relief Stick 14 g/100g; 4 g/100g; 4 g/100gthis 87917-0001-02 Kalahari 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

🏛️
2026
On the market since
Aug 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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
87917-0001-02 You're viewing this 1 TUBE in 1 BOX (87917-001-02) / 15 g in 1 TUBE (87917-001-01) 2026-08-07 Active
87917-0001-04 1 TUBE in 1 BOX (87917-001-04) / 30 g in 1 TUBE (87917-001-03) 2026-08-07 Active

Pack size FAQ

What quantity is in NDC 87917-0001-02?
NDC 87917-0001-02 is listed by the FDA — 1 tube in 1 box / 15 g in 1 tube.
What NDC number is used to bill for this package of Blaster Pain Relief Stick Menthol, Methyl Salicylate, Camphor 14 g/100g; 4 g/100g; 4 g/100g Stick?
Bill NDC 87917-0001-02 — the 11-digit billing format is 87917000102. 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 87917-001-02, 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: 87917-0001-02, written without dashes as 87917000102. 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 87917-0001-02, the first segment (87917) is the labeler code FDA assigned to Kalahari Rose, LLC; the middle segment (0001) 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: this package is listed as actively marketed, with no marketing end date reported by Kalahari Rose, 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 1 other package presentation of this same product, including 1 tube (87917-0001-04). 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?
Kalahari Rose, 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 31 words ▾

If condition worsens, or if symptoms persist for more than 7 dyas or clear up and return again withing a few days, discontinue use of this product and consult a doctor.

⏱️ Dosage and Administration 32 words ▾

Directions Adults and children 2 years of age and older: apply to affected area not more than 3-4 times daily. Children under 2 years of age: Do not use, consult a physician.

⚠️ Warnings 29 words ▾

Warnings For external use only Do not apply to wounds or damaged skin Avoid contact with eyes If pregnant, nursing, or under medical care, consult a physician before use.

🧪 Active Ingredient 16 words ▾

Active Ingredient Purpose Methyl Salicylate 14% Topical Analgesic Menthol 4% Topical Analgesic Camphor 4% Topical analgesic

🧪 Inactive Ingredients 60 words ▾

Inactive Ingredients Beeswax (Cera Alba), Butyrospermum Parkii (Shea) Butter, Cinnamomum Cassia Oil, Curcuma Longa (Turmeric) Root Oil, Cyprus Scariosus Root Oil, Eucalyptus Globulus Leaf Oil, Eugenia Caryophyllus (Clove) Bud Oil, Ferula Galbaniflua (Galbanum) Resin Oil, Hibuscus Abelmoschus Seed Oil, Hypericum Perforatum Oil, Kunzea Ambigua Branch/Leaf/Twig Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Melaleuca Leucadendron Cajaputi Oil, Withania Somnifera Root Extract.

🎯 Purpose 20 words ▾

Uses For the temporary relief of minor aches and pains of muscles and joints associated with strains, bruises and sprains.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 87916-0002-15 · Healthcare 87921-0111-01 · G.M.J →
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.