CANNA NUMB ROLL ON- lidocaine hydrochloride, menthol liquid

CANNA NUMB Roll On by

Drug Labeling and Warnings

CANNA NUMB Roll On by is a Otc medication manufactured, distributed, or labeled by Hempagenix, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts:

Active Ingredients

Lidocaine HCl 4%

Menthol 1%

Purpose

Topical Anesthetic

Topical Analgesic

Uses:

• temporarily relieves minor pain

Warnings:

For external use only.

Do not use

• on large areas of the body or on cut, irritated or swollen skin 
• on puncture wounds
• for more than one week without consulting a doctor

When using this product

• use only as directed. Read and follow directions and warnings on this package.
• Avoid contact with eyes and mucous membranes
• rare cases of serious burns have been reported with products of this type 
• do not apply to wounds or damaged, broken or irritated skin 
• do not bandage tightly or apply local heat (such as heating pads) or a medicated patch to the area of use
• a transient burning sensation may occur upon application but generally disappears in several days
• avoid applying into skin folds

Stop use and ask a doctor if

• conditions worsens
• redeness is present
• irritation develops 
• symptoms persist for more than 7 days or clear up and occur again within a few days
• you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied
• Flammable - keep away from fire or flame

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:

adults and children over 12 years:

• apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period
• massage into painful area until thoroughly absorbed into skin 
• children 12 years or younger: ask a doctor

Inactive Ingredients:

Aqua (Deionized Water), Arnica Montana Extract, Boswellia Serrata Extract, Cannabis Sativa (Hemp) Seed Oil, Carbomer, Citrus Aurantium Dulcis (Orange) Oil, Ethylhexylglycerin, Glucosamine Sulfate, Ilex Paraguayensis (Yerba Mate) Extract, Magnesium Sulfate, Methylsulfonylemthane (MSM), Phenoxyethanol, Polysorbate-20, Propylene Glycol, Salix Nigra (Willow) Bark Extract, Sd-Alcohol 40B, Triethanolamine.

Package Labeling:

INGREDIENTS AND APPEARANCE

CANNA NUMB ROLL ON 
lidocaine hydrochloride, menthol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72614-265
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	40 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA (UNII: O80TY208ZW)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
ORANGE OIL (UNII: AKN3KSD11B)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72614-265-02	73 mL in 1 CONTAINER; Type 0: Not a Combination Product	10/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/01/2018

Labeler - Hempagenix, LLC (081350922)