CBD MIST TOPICAL ANESTHETIC- lidocaine hydrochloride liquid
Meneks, Michael dba Doctor Energy, Inc.

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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CBD MIST Topical Anesthetic

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:

Label

CBD MIST TOPICAL ANESTHETIC
lidocaine hydrochloride liquid

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

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

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:73524-095-02	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/01/2019	02/28/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	12/01/2019	02/28/2022

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

Revised: 1/2022

Document Id: d58cad26-fb41-5bb3-e053-2995a90a0ceb

Set id: 15e7b1fc-cf17-4a5b-b114-747f3b126cf7

Version: 2

Effective Time: 20220114

Meneks, Michael dba Doctor Energy, Inc.