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Hempvana Pain Relief Trolamine Salicylate 10 g/100g Cream

by Telebrands Corp · 1 JAR in 1 CARTON (73287-001-01) / 119 g in 1 JAR
NDC 73287-0001-01
🏷️ FDA NDC (as labeled) 73287-001-01 billing pads the product segment with a zero
This package
Contains119 g in 1 jar Pack sizes2 compare ↓
Also comes in: 524 g 73287-0001-02
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) 73287-001-01
Product NDC 73287-001
11-digit billing NDC 73287000101
UNII H8O4040BHD
Application # M017
SPL Set ID 92a29553-a102-0a0e-e053-2a95a90ab24a
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-01-10
Route TOPICAL
Dosage form CREAM
Substance TROLAMINE SALICYLATE
Why two NDCs? The FDA registers this code as 73287-001-01 — 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 → 73287-0001-01. 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

LabelerTelebrands Corp
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code73287
First marketedJan 2019
Product typeHuman Otc Drug
Portfolio23 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?

Hempvana Pain Relief is a topical cream containing trolamine salicylate, an over-the-counter monograph product marketed without individual FDA review. Trolamine salicylate is a salt form of salicylate commonly used in topical pain relief products applied directly to the skin. This ingredient is typically used to help reduce minor aches and pains in muscles and joints.

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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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: 524 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
Hempvana Maximum Strength Pain Relief - Platinum 10 g/100g 73287-0021-01 TELEBRANDS 1 jar — — FDA listed —
Aspercreme Pain Relieving 10 g/100g 41167-0570-01 Chattem, 1 tube — — Discontinued —
Hempvana Maximum Strength Pain Relief Cream 10% Trolamine Salicylate 10 g/100g 73287-0032-01 TELEBRANDS 1 jar — — FDA listed —
Arthritis Relief GoodSense 10 g/100g 50804-0207-03 Geiss, 1 tube — — FDA listed —
Hempvana Pain Relief 10 g/100gthis 73287-0001-01 Telebrands 1 jar — — FDA listed —
Hempvana Maximum Strength Pain Relief 10 g/100g 73287-0022-01 TELEBRANDS 1 applicator — — FDA listed —
Hempvana Maximum Strength Pain Relief Cream 10% Trolamine Salicylate 10 g/100g 73287-0034-01 TELEBRANDS 1 jar — — FDA listed —
Mobisyl 10 g/100g 00225-0360-11 BF 100 g — — 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

🏛️
2019
On the market since
Jan 2019
📍
2026
Currently FDA-listed
7 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.

🔬 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 Hempvana Pain Relief (this brand).

Top reported reactions

Nausea9
Diarrhoea8
Dizziness8
Fatigue7
Back Pain5
Death5
Arthritis4

Reporter sex

78 reports

Serious outcomes

Death6
Life-threatening2
Disabling1
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 10 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
73287-0001-01 You're viewing this 1 JAR in 1 CARTON (73287-001-01) / 119 g in 1 JAR 2019-01-10 Active
73287-0001-02 524 g in 1 BOTTLE, PUMP (73287-001-02) 2024-02-22 Active

Pack size FAQ

What quantity is in NDC 73287-0001-01?
NDC 73287-0001-01 is listed by the FDA — 1 jar in 1 carton / 119 g in 1 jar.
What NDC number is used to bill for this package of Hempvana Pain Relief Trolamine Salicylate 10 g/100g Cream?
Bill NDC 73287-0001-01 — the 11-digit billing format is 73287000101. 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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 73287-001-01, 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: 73287-0001-01, written without dashes as 73287000101. 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 73287-0001-01, the first segment (73287) is the labeler code FDA assigned to Telebrands Corp; the middle segment (0001) 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: this package is listed as actively marketed, with no marketing end date reported by Telebrands Corp. 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 524 g (73287-0001-02). 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?
Telebrands Corp 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 📋 Description
🎯 Indications and Usage 19 words ▾

Uses temporarily relieves minor pain associated with: • arthritis • simple backache • muscle strains • sprains • bruises

⏱️ Dosage and Administration 50 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: Consult a physician Massage into painful area until thoroughly absorbed into skin. Repeat as necessary, but no more than 4 times daily.

⚠️ Warnings 150 words ▾

Warnings For external use only Allergy alert : If prone to allergic reaction from aspirin or salicylates, consult a doctor before use. When using this product Use only as directed. Read and follow all directions and warnings on this label.

Do not bandage tightly or apply local heat (such as heating pads) to the area of use. Avoid contact with eyes or mucous membranes. Do not apply to wounds or damaged, broken or irritated skin.

Do not use at the same time as other topical analgesics. Stop use and ask a doctor if Condition worsens Symptoms persist for more than 7 days or clear up and occur again within a few days Redness is present or irritation develops If pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children and pets.

If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 5 words ▾

Active Ingredient: Trolamine Salicylate 10%

🧪 Inactive Ingredients 57 words ▾

Inactive Ingredients Water/Aqua, Ethylhexyl Stearate, Butylene Glycol, Dimethicone, Stearic Acid, Caprylic/Capric Triglyceride, Hemp Seed Oil (Hemp Seed Oil), Glyceryl Stearate, PEG-100 Stearate, Cetostearyl Alcohol, Sunflower Oil, Allantoin, Tocopheryl Acetate, Ethylhexylglycerin, Isohexadecane, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Caprylyl Glycol, Hexylene Glycol, Polysorbate 80, Disodium EDTA, D&C Green No. 5 (CI 61570), Sodium Hydroxide, Phenoxyethanol

🎯 Purpose 5 words ▾

Purpose Trolamine Salicylate 10%................Topical Analgesic

📋 Description 100 words ▾

Hempvana ® Pain Relief Cream absorbs quickly and goes to work instantly. Its unique formula includes a proven active ingredient plus the moisturizing benefit of cold pressed hemp seed* extract for soothing relief to back, neck, shoulders, feet, wrists, calves and more. Maximum Strength Odor Free Non-Irritating No Burning Non Greasy TAMPER EVIDENT: Do not use if safety seal on cap is broken or missing.

For more information, visit www.HempvanaStore.com *Complies with Federal Law. Hemp seed extract in the form of oil made by cold-pressing industrial hemp seeds. cultivar. Dist. by: Telebrands Corp.

79 Two Bridges Road, Fairfield, NJ 07004

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 73284-0508-00 · Innovation 73287-0004-01 · Telebrands →
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.