EVERLIT CARE PRODUCTS BURN RELIEF- lidocaine hydrochloride spray

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Lidocaine HCI: 2%

PURPOSE

Purpose

Topical Pain Relief

INDICATIONS & USAGE

Uses

Temporary pain relief associated with minor burns.

WARNINGS

Warnings

For external use only.

DO NOT USE

Do not use

• in the eyes
• in large quantities, particularly over raw or blistered areas
• if allergic to any ingredient
• on deep puncture wounds or serious burns

STOP USE

Stop use and seek medical help

if the condition worsens or persist for more than 7 days or clears up and returns

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Directions

Spray and even layer of brun spray over cleaned affected area not more than 3 to 4 times daily

Chilrdren under 12 years of age: ask a doctor

Other Information

Store at room temperature

INACTIVE INGREDIENT

Inactive ingredients

Aminomethyl Propanol, Glycerin, Hydroxypropyl Methylcellulose,  Melaleuca Alterniflia (Tea Tree) Leaf Oil, Octoxyol 9, PEG-40 Hydrogenated Castor Oil, Phenoxyethanol, Polyethylene Glycol,  Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EVERLIT CARE PRODUCTS BURN RELIEF 
lidocaine hydrochloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83807-032
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HYDROXYPROPYL METHYLCELLULOSE (UNII: 3NXW29V3WO)
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)
OCTOXYNOL 9 (UNII: 7JPC6Y25QS)
PEG-40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
AMINOMETHYL PROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83807-032-01	59.1 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/04/2026

Labeler - EVERLIT GLOBAL INC. (122311450)

Establishment
Name	Address	ID/FEI	Business Operations
Nantong Health & Beyond Hygienic Products Inc.		421280161	manufacture(83807-032)