NUMBING CREAM- lidocaine cream

Numbing Cream by

Drug Labeling and Warnings

Numbing Cream by is a Otc medication manufactured, distributed, or labeled by Kanamed Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Lidocaine 5%

INDICATIONS & USAGE

Temporarily relieves minor pain

INACTIVE INGREDIENT

• Hemp seed oil
• Clove Oil
• Tea Tree Oil
• Glycerine
• Stearic Acid
• EDTA
• Arcel 165
• Carbopol U-10,
• Cetyl Alcohol
• BHT
• Cetearyl Alcohol
• Cetearyl Glucoside
• Phenoxyethanol
• Ethylhexlglycerin
• DM Water
• Cyclopentasiloxane
• Phenyl Trimethicone
• Dimethiconol
• C12-15 Alkyl Benzoate
• Dimethicone Crosspolymer
• Caustic Soda/Sodium Hydroxide
• Capric Caprylic Triglyceride

DOSAGE & ADMINISTRATION

Adults and children over 12 years of age: Apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period.

Children 12 years or younger: consult a doctor.

WARNINGS

• For external use only
• Only use as directed
• Do not allow contact with eyes
• Do not bandage or apply local heat such as heating pads to the area of use

STOP use and ask a doctor if:

• symptoms last more than 7 days or clear up and occur again within a few days
• condition worsens

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

PURPOSE

Temporarily relieves minor pain​

OTHER SAFETY INFORMATION

Store at room temperature

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NUMBING CREAM 
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73239-1902
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	5 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
HEMP (UNII: TD1MUT01Q7)
WATER (UNII: 059QF0KO0R)	1 mg  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73239-1902-1	100 mL in 1 TUBE; Type 0: Not a Combination Product	10/16/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/16/2019

Labeler - Kanamed Inc. (117131580)

Registrant - Kanamed Inc. (117131580)