Hempvana Cold As Ice

Manufacturer
Telebrands Corp | Southeast Holdings Corp
Effective date
2025-11-12
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:43:37

Label at a glance#

ProductHempvana Cold As Ice 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

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

Questions?

OTC - QUESTIONS SECTION

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

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73287-004-01Hempvana Cold As IcePain Relief1 in 1 CARTONGEL16
73287-004-01Hempvana Cold As IcePain Relief74 mL in 1 BOTTLE, WITH APPLICATORGEL746

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73287-00473287-004-01

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-11-20full-release2026-06-01 00:38:25

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 Cold As Ice Pain ReliefMENTHOLTelebrands Corp95e84bb9-ba2e-5009-e053-2995a90a43622025-11-12WarningsExact identifier
ndc (package): 73287-004-01
ndc (product): 73287-004
ndc11 (package): 73287000401
spl id: 436cde39-5a39-ba83-e063-6394a90a06d8
spl set id: 95e84bb9-ba2e-5009-e053-2995a90a4362

Reported adverse events (FAERS/openFDA)#

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