CBD MIST TOPICAL ANESTHETIC- lidocaine hydrochloride liquid

CBD MIST Topical Anesthetic by

Drug Labeling and Warnings

CBD MIST Topical Anesthetic by is a Otc medication manufactured, distributed, or labeled by Meneks, Michael dba Doctor Energy, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Lidocaine HCl 4.00%

Purpose

Topical Analgesic

Uses:

For temporary relief of pain.

Warnings:

For external use only.

Avoid contact with eyes.
If symptoms persist for more than seven days, discontinue use and consult physician.

Keep out of reach of children.

• If swallowed, consult physician.

Do not use

• in large quantities, particularly over raw surfaces or blistered areas.

If pregnant or breast feeding,

contact physician prior to use.

Directions:

Adults and children two-years of age or older: Apply to affected area not more than three to four times daily.
Children under two-years of age: consult a physician.

Additional Information:

Store at room temperature.

Other Ingredients:

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Cannabis Sativa (Full Spectrum Hemp) Oil, Ethylhexylglycerin, Isopropyl Alcohol, Methylsulfonylmethane (MSM), Phenoxyethanol, Polysorbate 20, Rosmarinus Officinalis (Rosemary) Oil, Simmondsia Chinensis (Jojoba) Oil.

Package Labeling:

INGREDIENTS AND APPEARANCE

CBD MIST TOPICAL ANESTHETIC 
lidocaine hydrochloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73524-095
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

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
ROSEMARY (UNII: IJ67X351P9)
JOJOBA OIL (UNII: 724GKU717M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73524-095-02	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	12/01/2019

Labeler - Meneks, Michael dba Doctor Energy, Inc. (009963305)