FOOT HANGOVER- lidocaine hcl liquid 
Ari Brands, Llc

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.

----------

FOOT HANGOVER

Drug Facts

Active ingredients (in each bottle)

Lidocaine HCL 4%

Purpose

External analgesic

Uses

For the temporary relief of pain and itching due to minor burns, sunburn, minor cuts, abrasions, insect bites, and minor skin irritations.

Warnings

For external use only. Avoid contact with eyes.

Flammable: Do not use while smoking or near heat or flame.

Do not use in large quantities, particularly over raw surfaces or blistered areas, on large areas of the body or on a cut, irritated or swollen skin, or for more than one week without consulting a physician.

Stop use and ask a doctor if: conditions worsen, symptoms persist for more than 7 days or clear up and occur again within a few days.

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 the Poison Control Center right away.

Directions
adults and children 2 years and olderapply externally to the affected area up to 3 to 4 times a day 
children under 2 yearsask a doctor

Other Information

Contents under pressure. Do not store at temperatures above 120° F

When using this product; Use only as directed. Do not puncture or incinerate.

Inactive Ingredients

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Distilled water), Parfum (Fragrance), Potassium Sorbate, Saccharide Isomerate, SD-Alcohol 40B

Foot Hangover

Los Angeles, California 90064

(310)294-8956

Packaging

FootHngover1

FOOT HANGOVER 
lidocaine hcl liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71436-0024
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SACCHARIDE ISOMERATE (UNII: W8K377W98I)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71436-0024-4118 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/01/2018
Labeler - Ari Brands, Llc (080658382)

Revised: 1/2018
Document Id: 0dbc1594-d0ff-4e73-b1bb-81b49221f892
Set id: 50b65dab-e5b5-42b1-a1a3-719bf070b0ba
Version: 2
Effective Time: 20180131
 
Ari Brands, Llc