FOOT HANGOVER- lidocaine hcl liquid

FOOT HANGOVER by

Drug Labeling and Warnings

FOOT HANGOVER by is a Otc medication manufactured, distributed, or labeled by Ari Brands, Llc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

Keep out of reach of children and pets. If swallowed, get medical help or contact the Poison Control Center right away.

DOSAGE & ADMINISTRATION

• adults and children 2 years and older: apply externally to the affected area up to 3 to 4 times a day
• children under 2 years: ask 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

SPL UNCLASSIFIED SECTION

Foot Hangover

Los Angeles, California 90064

(310)294-8956

Packaging

INGREDIENTS AND APPEARANCE

FOOT HANGOVER 
lidocaine hcl liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71436-0024
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SACCHARIDE ISOMERATE (UNII: W8K377W98I)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71436-0024-4	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	01/01/2018

Labeler - Ari Brands, Llc (080658382)