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 TypeHUMAN OTC DRUGItem Code (Source)NDC:73524-095
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73524-095-0260 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34812/01/2019
Labeler - Meneks, Michael dba Doctor Energy, Inc. (009963305)

Revised: 12/2019
Document Id: 9aec3cbc-2bf7-121b-e053-2a95a90af4d1
Set id: 15e7b1fc-cf17-4a5b-b114-747f3b126cf7
Version: 1
Effective Time: 20191230
 
Meneks, Michael dba Doctor Energy, Inc.