HEMPVANA ULTRA STRENGTH PAIN RELIEF GEL PLATINUM - ARTHRITIS- menthol 8% gel

Hempvana Ultra Strength Pain Relief Gel - Arthritis by

Drug Labeling and Warnings

Hempvana Ultra Strength Pain Relief Gel - Arthritis by is a Otc medication manufactured, distributed, or labeled by Telebrands Corp, Neutraderm, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Menthol 8%

Purpose

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

Uses

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

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.

Directions

■ 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

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?

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

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)

INGREDIENTS AND APPEARANCE

HEMPVANA ULTRA STRENGTH PAIN RELIEF GEL PLATINUM - ARTHRITIS 
menthol 8% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73287-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	8 g  in 8 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ALCOHOL (UNII: 3K9958V90M)
SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
MELISSA OFFICINALIS FLOWERING TOP (UNII: 5JQG17B06J)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
CAMPHOR, (-)- (UNII: 213N3S8275)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
TURMERIC (UNII: 856YO1Z64F)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73287-030-01	1 in 1 CARTON	09/02/2024
1		85 g in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	09/02/2024

Labeler - Telebrands Corp (177266558)

Establishment
Name	Address	ID/FEI	Business Operations
Neutraderm, Inc.		146224444	manufacture(73287-030)