HEMPVANA MAXIMUM STRENGTH PAIN RELIEF - PLATINUM- trolamine salicylate cream

Hempvana Maximum Strength Pain Relief - Platinum by

Drug Labeling and Warnings

Hempvana Maximum Strength Pain Relief - Platinum 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

Trolamine Salicylate 10%

Purpose

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

Uses

temporarily relieves minor pain associated with:

• arthritis
• simple backache
• muscle strains
• sprains
• bruises

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 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.

Inactive ingredients

Water/Aqua/Eau, Ethylhexyl Stearate, Cannabis Sativa (Hemp) Seed Oil, Butylene Glycol, Stearic Acid, DImethicone, Caprylic/Capric Trigylceride, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Helianthus Annuus (Sunflower) Seed Oil, Glycerin, Aloe Barbadensis Leaf Extract, Arnica Montana Flower Extract, Curcuma Longa (Turmeric) Root Extract, Dimethyl Sulfone, Tocopheryl Acetate, Phenoxyethanol, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Caprylyl Glycol, Isohexadecane, Ethylhexylglycerin, Hexylene Glycol, Allantoin, Mannitol, Microcrystalline Cellulose, Iron Oxides Yellow (CI 77492), Tocopherol, Hydroxypropyl Methylcellulose, Ubiquinone, Polysorbate 80, Sodium Hydroxide, Disodium EDTA, Yellow 6 (CI 15985), Blue 1 (CI 42090)

Questions?

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

PRINCIPAL DISPLAY PANEL

Hempvana

Maximum Strength Pain Relief Cream

Platinum

+4x Hemp* Seed Oil

For Moisturization

Trolamine Salicylate 10%

For Pain

Net Wt. 4 oz (119 g)

*Compared to original Hempvana Pain Relief Cream

INGREDIENTS AND APPEARANCE

HEMPVANA MAXIMUM STRENGTH PAIN RELIEF - PLATINUM 
trolamine salicylate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73287-021
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TROLAMINE SALICYLATE (UNII: H8O4040BHD) (SALICYLIC ACID - UNII:O414PZ4LPZ)	TROLAMINE SALICYLATE	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
TURMERIC (UNII: 856YO1Z64F)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
UBIDECARENONE (UNII: EJ27X76M46)
ALLANTOIN (UNII: 344S277G0Z)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
STEARIC ACID (UNII: 4ELV7Z65AP)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
DIMETHICONE (UNII: 92RU3N3Y1O)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
SUNFLOWER OIL (UNII: 3W1JG795YI)
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
TOCOPHEROL (UNII: R0ZB2556P8)
GLYCERIN (UNII: PDC6A3C0OX)
ISOHEXADECANE (UNII: 918X1OUF1E)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
WATER (UNII: 059QF0KO0R)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
PEG-100 STEARATE (UNII: YD01N1999R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73287-021-01	1 in 1 CARTON	01/14/2022
1		119 g in 1 JAR; Type 0: Not a Combination Product
2	NDC: 73287-021-02	524 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/22/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/14/2022

Labeler - TELEBRANDS CORP (177266558)

Establishment
Name	Address	ID/FEI	Business Operations
Neutraderm, Inc.		146224444	manufacture(73287-021)