Hempvana Ultra Strength Pain Relief Cream - Night

Hempvana Ultra Strength Pain Relief Cream - Night by

Drug Labeling and Warnings

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

Drug Details [pdf]

HEMPVANA ULTRA STRENGTH PAIN RELIEF CREAM - NIGHT- lidocaine 4% cream 
Telebrands Corp

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Hempvana Ultra Strength Pain Relief Cream - Night

Active Ingredient

Lidocaine 4%

Purpose

Lidocaine 4%.......................Topical Analgesic

Uses

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.

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

Questions?

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

Hempvana

Ultra Strength

Pain Relief

Cream

Night with Calming Lavender

+ Hemp Seed Oil

Lidocaine 4%

Net Wt. 4 OZ (119 g)

1

2

HEMPVANA ULTRA STRENGTH PAIN RELIEF CREAM - NIGHT 
lidocaine 4% cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73287-017
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
ALLANTOIN (UNII: 344S277G0Z)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
MELATONIN (UNII: JL5DK93RCL)  
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PEG-100 STEARATE (UNII: YD01N1999R)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
PIPER METHYSTICUM ROOT (UNII: BOW48C81XP)  
LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
ETHYLHEXYL PALMITATE (UNII: 2865993309)  
COCOA BUTTER (UNII: 512OYT1CRR)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73287-017-011 in 1 CARTON05/24/202112/31/2022
1119 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34805/24/202112/31/2022
Labeler - Telebrands Corp (177266558)
Establishment
NameAddressID/FEIBusiness Operations
Neutraderm, Inc.146224444manufacture(73287-017)

Revised: 12/2022
 

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