FDA.reportPublic FDA data

Hempvana Maximum Strength Pain Relief Cream 10% Trolamine Salicylate

Manufacturer
TELEBRANDS CORP | Neutraderm, Inc.
Effective date
2025-02-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:54:28

Label at a glance#

ProductHempvana Maximum Strength Pain Relief Cream 10% Trolamine Salicylate
Active ingredientTROLAMINE SALICYLATE
Label structure8 sections

Indications and uses

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

Dosage and administration

Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily using roller ball applicator Children under 2 years of age: consult a physician

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Trolamine Salicylate 10%

Purpose

OTC - PURPOSE SECTION

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

Uses

INDICATIONS & USAGE SECTION

temporarily relieves minor pain associated with:

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

Warnings

WARNINGS SECTION

For external use only

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 area not more than 3 to 4 times daily using roller ball applicator
  • Children under 2 years of age:consult a physician

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua/Eau, Ethylhexyl Stearate,Butylene Glycol, Dimethicone, Stearic Acid, Caprylic/CapricTriglyceride, Glyceryl Stearate, Hemp (Cannabis Sativa) Seed Oil,PEG-100 Stearate, Cetearyl Alcohol, Magnesium Sulfate, Sunflower(Helianthus Annuus) Seed Oil, Allantoin, Acrylates/C10-30 AlkylAcrylate Crosspolymer, Tocopheryl Acetate, Sodium Acrylate/SodiumAcryloyldimethyl Taurate Copolymer, Caprylyl Glycol, Isohexadecane, Hexylene Glycol, Ethylhexylglycerin, Sodium Hydroxide,Polysorbate 80, Disodium EDTA, Phenoxyethanol

Questions?

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hempvana Brand

Maximum Strength Pain Relief Cream

10% Trolamine Salicylate

Epsom salt & Hemp Seed Oil for moisturization

For Moisturization

Net Wt. 3 OZ (85 g)

Outer BoxOuter Box

InnerInner

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73287-032-01Hempvana Maximum Strength Pain Relief Cream 10% Trolamine Salicylate85 g in 1 JARCREAM851
73287-032-01Hempvana Maximum Strength Pain Relief Cream 10% Trolamine Salicylate1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73287-032HEMPVANA MAXIMUM STRENGTH PAIN RELIEF CREAM 10% TROLAMINE SALICYLATE (TROLAMINE SALICYLATE) CREAM [TELEBRANDS CORP]1Current NDC, 2 package rows20250207_2d685602-5cd6-3b36-e063-6394a90a3c5d.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73287-03273287-032-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
MAGNESIUM SULFATEDE08037SABIACT
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW)1DXE3F3OZXIACT
CAPRYLYL GLYCOL00YIU5438UIACT
POLYSORBATE 806OZP39ZG8HIACT
SODIUM HYDROXIDE55X04QC32IIACT
SUNFLOWER OIL3W1JG795YIIACT
WATER059QF0KO0RIACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
PEG-100 STEARATEYD01N1999RIACT
STEARIC ACID4ELV7Z65APIACT
ALLANTOIN344S277G0ZIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
DIMETHICONE92RU3N3Y1OIACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
TROLAMINE SALICYLATEH8O4040BHDACTIB
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
CETEARYL ALCOHOL2DMT128M1SIACT
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S AT 0.5%)YY2HMJ9NZFIACT
ISOHEXADECANE918X1OUF1EIACT

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 Maximum Strength Pain Relief Cream 10% Trolamine SalicylateTROLAMINE SALICYLATETELEBRANDS CORP2d685602-5cd6-3b36-e063-6394a90a3c5d2025-02-05WarningsExact identifier
ndc (package): 73287-032-01
ndc (product): 73287-032
ndc11 (package): 73287003201
spl id: 2d686088-00da-d0d1-e063-6294a90acf89
spl set id: 2d685602-5cd6-3b36-e063-6394a90a3c5d

Reported adverse events (FAERS/openFDA)#

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