2.0% LIDOCAINE BURN- lidocaine hydrochloride spray

2.0% LIDOCAINE BURN by

Drug Labeling and Warnings

2.0% LIDOCAINE BURN by is a Otc medication manufactured, distributed, or labeled by Universal Distribution Center LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

​Drug Facts

​Active ingredient

Lidocaine HCl 2.0%

​Purpose

Topical pain relief

​Uses

Temporary pain relief associated with minor burns

​Warnings

​For external use only.

Do not use  in large quantities, particularly over raw or blistered area  near eyes, if this happens rinse thoroughly with water

​Stop use and ask a doctor if ​the condition worsens or persists for more than 7 days or clears up and returns.

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

​Directions

spray an even layer of burn spray over cleaned affected area not more than 3-4 times daily  not to be used on children under 12 years of age

Inactive ingredients

AMINOMETHYL PROPANOL, GLYCERIN, HYDROXYPROPYL METHYLCELLULOSE, MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL, OCTOXYNOL-9, PEG-40 HYDROGENATED CASTOR OIL, PHENOXYETHANOL, PROPYLENE GLYCOL, WATER

SPL UNCLASSIFIED SECTION

✓ Instant Cooling Relief

✓ Soothes Minor Burns & Sunburns

Store at 68°-77°F (20°-25°C)

​Mfd for and Distributed by:
Universal Distribution Center LLC
330 Applegarth Road,
Monroe Township, NJ 08831

www.universaldc.com

MADE IN CHINA

Packaging

INGREDIENTS AND APPEARANCE

2.0% LIDOCAINE BURN 
lidocaine hydrochloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-441
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
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
GLYCERIN (UNII: PDC6A3C0OX)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
TEA TREE OIL (UNII: VIF565UC2G)
OCTOXYNOL-9 (UNII: 7JPC6Y25QS)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-441-02	59.1 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/19/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/19/2026

Labeler - Universal Distribution Center LLC (019180459)