HEMPVANA COLD AS ICE PLATINUM PAIN RELIEF- menthol gel

Hempvana Cold As Ice Platinum by

Drug Labeling and Warnings

Hempvana Cold As Ice Platinum by is a Otc medication manufactured, distributed, or labeled by Telebrands Corp, A.I.G. TECHNOLOGIES, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient:

Menthol USP 8% w/w

Purpose

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

Uses

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

simple backache arthritis strains bruises sprains

Warnings

For external use only

Flammable:Keep away from excessive heat or open flame

When using this product, avoid contact with eyes.

• 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

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

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

Directions

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.

Inactive Ingredients

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?

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

Packaging

INGREDIENTS AND APPEARANCE

HEMPVANA COLD AS ICE PLATINUM  PAIN RELIEF
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73287-033
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	8 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BOSWELLIA CARTERII OIL (UNII: 67ZYA5T02K)
WATER (UNII: 059QF0KO0R)
ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
CALENDULA OFFICINALIS WHOLE (UNII: PFR03EBU0H)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
MELISSA OFFICINALIS (UNII: YF70189L0N)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
CURCUMA LONGA (TURMERIC) ROOT (UNII: 856YO1Z64F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73287-033-01	74 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	03/24/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/24/2025

Labeler - Telebrands Corp (177266558)

Establishment
Name	Address	ID/FEI	Business Operations
A.I.G. TECHNOLOGIES, INC.		086365223	manufacture(73287-033)