FDA.reportPublic FDA data

Hempvana Cold As Ice Platinum

Manufacturer
Telebrands Corp | A.I.G. TECHNOLOGIES, INC.
Effective date
2025-03-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:57:47

Label at a glance#

ProductHempvana Cold As Ice Platinum Pain Relief
Active ingredientMENTHOL
Label structure9 sections

Indications and uses

temporarily relief of minor aches and pains of muscles and joints associated with: • simple backache • arthritis • strains • bruises • sprains

Dosage and administration

Adults : Apply to affected are not more than 3 to 4 times daily. If produce comes in contact with hands, wash with soap and water. For children under 18 years of age: Consulta a physician.

Storage and handling

Store tightly closed in a cool dry place.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Menthol USP 8% w/w

Purpose

OTC - PURPOSE SECTION

Menthol USP 8% w/w................Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

temporarily relief of minor aches and pains of muscles and joints associated with:

• simple backache • arthritis • strains • bruises • sprains

Warnings

WARNINGS SECTION

For external use only

Flammable:Keep away from excessive heat or open flame

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes.

OTC - DO NOT USE SECTION

  • Do nut use in large quantities, particularly over raw surfaces or blistered areas.
  • Do not apply to wounds or damaged skin
  • Do not bandage tightly

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Adults: Apply to affected are not more than 3 to 4 times daily. If produce comes in contact with hands, wash with soap and water.

For children under 18 years of age:Consulta a physician.

STORAGE AND HANDLING SECTION

Store tightly closed in a cool dry place.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Aloe Barbadensis Leaf Extract, Cannabis Sativa Seed Oil, Camphor, Arnica Montana Flower Extract, Arctium Lappa (Burdock) Root Extract, Boswellia Carteril Resin Extract, Calendula Officinalis Extract, Camellia Sinensis Leaf Extract, Ilex Paraguariensis Leaf Extract, Melissa Officinalis (Lemon Balm) Leaf Extract, Curcuma Longo (Turmeric) Root Extract, Isopropyl Myristate, Tocopheryl Acetate, Glycerin, Silica, Carbomer,Triethanolamine, FD&C Blue No.1, FD&C Yellow No. 5

Questions?

OTC - QUESTIONS SECTION

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

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73287-033-01Hempvana Cold As Ice PlatinumPain Relief74 mL in 1 BOTTLE, WITH APPLICATORGEL741

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73287-033HEMPVANA COLD AS ICE PLATINUM PAIN RELIEF (MENTHOL) GEL [TELEBRANDS CORP]11 package rows20250327_312e6bde-150b-23bc-e063-6394a90a4d54.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73287-03373287-033-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
BOSWELLIA CARTERII OIL67ZYA5T02KIACT
WATER059QF0KO0RIACT
ARCTIUM LAPPA ROOT597E9BI3Z3IACT
ALOE VERA LEAFZY81Z83H0XIACT
ILEX PARAGUARIENSIS LEAF1Q953B4O4FIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
CALENDULA OFFICINALIS WHOLEPFR03EBU0HIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CAMPHOR (NATURAL)N20HL7Q941IACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL ALCOHOLND2M416302IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
MELISSA OFFICINALISYF70189L0NIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
MENTHOLL7T10EIP3AACTIB
TRIETHANOLAMINE9O3K93S3TKIACT
CURCUMA LONGA (TURMERIC) ROOT856YO1Z64FIACT

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
312e6bf1-a72b-5938-e063-6294a90aaea8312e6bde-150b-23bc-e063-6394a90a4d542025-03-25WarningsExact identifier
spl id: 312e6bf1-a72b-5938-e063-6294a90aaea8
spl set id: 312e6bde-150b-23bc-e063-6394a90a4d54

Reported adverse events (FAERS/openFDA)#

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