HEMPVANA ULTRA STRENGTH PAIN RELIEF - OVERNIGHT- lidocaine cream

Hempvana Ultra Strength Pain Relief - Overnight by

Drug Labeling and Warnings

Hempvana Ultra Strength Pain Relief - Overnight by is a Otc medication manufactured, distributed, or labeled by Telebrands Corp, Neutraderm, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Lidocaine 4%

Purpose

Lidocaine 4%...... Topical Analgesic

Uses

For the temporary relief of pain

Warnings

For external use only

Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

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.
■ do not use in large quantities, particularly over raw surfaces or blistered areas.

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

If pregnant or breast-feeding, ask a health professional before use.

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

Directions

■ For Use By Adults Only
■ Apply generously to affected area
■ Massage into painful area until thoroughly absorbed into skin.
■ Repeat as necessary, but no more than 4 times daily.

Inactive Ingredients

Water/Aqua/Eau, Propylene Glycol, Ethylhexyl Palmitate, Stearic Acid, Dimethicone, PEG-100 Stearate, Glyceryl Stearate, Cetearyl Alcohol, Hemp (Cannabis Sativa) Seed Oil, Lavender (Lavandula Angustifolia) Oil, Cocoa (Theobroma Cacao) Seed Butter, Lavender (Lavandula Angustifolia) Flower Extract, English/Roman Chamomile (Chamaemelum Nobile) Flower Extract, Melatonin, Kava (Piper Methysticum) Root Extract, Allantoin, Potassium Cetyl Phosphate, Glycerin, Tocopheryl Acetate, Phenoxyethanol, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Caprylyl Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Isohexadecane, Hexylene Glycol, Ethylhexylglycerin, Polysorbate 80, Disodium EDTA, Sodium Hydroxide, Red 4 (CI 14700), Blue 1 (CI 42090)

Questions

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

PRINCIPAL DISPLAY PANEL

Hempvana

Ultra Strength

Pain Relief

Cream

Lidocaine 4%

Overnight

Lavender Scent

Melatonin

+ Hemp Seed Oil

For Moisturization

Net Wt. 3oz (85 g)

INGREDIENTS AND APPEARANCE

HEMPVANA ULTRA STRENGTH PAIN RELIEF - OVERNIGHT 
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73287-029
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PEG-100 STEARATE (UNII: YD01N1999R)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
STEARIC ACID (UNII: 4ELV7Z65AP)
LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
WATER (UNII: 059QF0KO0R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERIN (UNII: PDC6A3C0OX)
ISOHEXADECANE (UNII: 918X1OUF1E)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DIMETHICONE (UNII: 92RU3N3Y1O)
LAVENDER OIL (UNII: ZBP1YXW0H8)
ALLANTOIN (UNII: 344S277G0Z)
PIPER METHYSTICUM ROOT (UNII: BOW48C81XP)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
COCOA BUTTER (UNII: 512OYT1CRR)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
MELATONIN (UNII: JL5DK93RCL)
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73287-029-01	1 in 1 CARTON	01/30/2024
1		85 g in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/30/2024

Labeler - Telebrands Corp (177266558)

Establishment
Name	Address	ID/FEI	Business Operations
Neutraderm, Inc.		146224444	manufacture(73287-029)