FDA.reportPublic FDA data

Hempvana Ultra Strength Pain Relief Gel Platinum - Arthritis

Manufacturer
Telebrands Corp | Neutraderm, Inc.
Effective date
2024-09-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:19:06

Label at a glance#

ProductHempvana Ultra Strength Pain Relief Gel Platinum - Arthritis
Active ingredientMENTHOL
Label structure8 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints

Dosage and administration

■ Adults and children 2 years of age and older: apply to affected areanot more than 3 to 4 times daily. ■ Children under 2 years of age: consult a physician

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 8%

Purpose

OTC - PURPOSE SECTION

Menthol 8%....................Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints

Warnings

WARNINGS SECTION

For external use only

OTHER SAFETY INFORMATION

Allergy alert:If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

OTC - WHEN USING SECTION

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.

OTC - STOP USE SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding,ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Adults and children 2 years of age and older: apply to affected areanot more than 3 to 4 times daily.

■ Children under 2 years of age: consult a physician

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua/Eau, Alcohol Denat., Isopropyl Myristate, Sodium Hydroxide, Silica Silylate, Dimethyl Sulfone, Glucosamine Sulfate, Sodium Chondroitin Sulfate, Cannabis Sativa (Hemp) Seed Oil, Camphor, Aloe Barbadensis Leaf Extract, Arctium Lappa Root Extract, Arnica Montana Flower Extract, Calendula Officinalis Flower Extract, Camellia Sinensis Leaf Extract, Curcuma Longa (Turmeric) Root Extract, Ilex Paraguariensis Leaf Extract, Melissa Officinalis Flower/Leaf/Stem Extract, Phenoxyethanol, Carbomer, Ethylhexylglycerin, Disodium EDTA, Glycerin, Tocopheryl Acetate, Yellow 5 (CI 19140), Blue 1 (CI 42090)

Questions?

OTC - QUESTIONS SECTION

Questions? Call (855) 877-4503 (M-F, 9am-5pm EST)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

​Hempvana

Ultra Strength

Pain Relief

Menthol 8%

Gel

Platinum

Arthritis

+ 4 x Hemp Seed Oil for Moisturization

Net Wt. 3 OZ (85 g)

BOXBOXJarJar

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73287-030-01Hempvana Ultra Strength Pain Relief Gel Platinum - Arthritis85 g in 1 JARGEL853
73287-030-01Hempvana Ultra Strength Pain Relief Gel Platinum - Arthritis1 in 1 CARTONGEL13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73287-030HEMPVANA ULTRA STRENGTH PAIN RELIEF GEL PLATINUM - ARTHRITIS (MENTHOL 8%) GEL [TELEBRANDS CORP]3Current NDC, 2 package rows20240907_c22cf1a5-0d5d-5ea5-e053-2995a90a333b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73287-03073287-030-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
SODIUM HYDROXIDE55X04QC32IIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
ALCOHOL3K9958V90MIACT
SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW)H5BJH23Z9AIACT
ALOE VERA LEAFZY81Z83H0XIACT
ARCTIUM LAPPA ROOT597E9BI3Z3IACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
MELISSA OFFICINALIS FLOWERING TOP5JQG17B06JIACT
PHENOXYETHANOLHIE492ZZ3TIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
GLYCERINPDC6A3C0OXIACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
GLUCOSAMINE SULFATE1FW7WLR731IACT
CAMPHOR, (-)-213N3S8275IACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
TURMERIC856YO1Z64FIACT
ILEX PARAGUARIENSIS LEAF1Q953B4O4FIACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
FD&C BLUE NO. 1H3R47K3TBDIACT
MENTHOLL7T10EIP3AACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Hempvana Ultra Strength Pain Relief Gel Platinum - ArthritisMENTHOL 8%Telebrands Corpc22cf1a5-0d5d-5ea5-e053-2995a90a333b2024-09-02WarningsExact identifier
ndc (package): 73287-030-01
ndc (product): 73287-030
ndc11 (package): 73287003001
spl id: 21750d88-ebdb-1dca-e063-6294a90ab604
spl set id: c22cf1a5-0d5d-5ea5-e053-2995a90a333b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.