HEMPVANA COLD AS ICE PAIN RELIEF- menthol gel

Hempvana Cold As Ice by

Drug Labeling and Warnings

Hempvana Cold As Ice 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

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?

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

Packaging

INGREDIENTS AND APPEARANCE

HEMPVANA COLD AS ICE  PAIN RELIEF
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73287-004
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
WATER (UNII: 059QF0KO0R)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
FRANKINCENSE (UNII: R9XLF1R1WM)
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)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
MELISSA OFFICINALIS (UNII: YF70189L0N)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73287-004-01	1 in 1 CARTON	06/11/2019
1		74 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	06/11/2019

Labeler - Telebrands Corp (177266558)

Establishment
Name	Address	ID/FEI	Business Operations
A.I.G. Technologies Incorporated		171837367	manufacture(73287-004)