0.5% LIDOCAINE BURN RELIEF- lidocaine hydrochloride gel 
Nantong Health & Beyond Hygienic Products Inc.

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43473-099 - 0.5% LIDOCAINE BURN RELIEF GEL

Drug Facts

Active ingredient

Lidocaine HCl 0.5%

Purpose

External analgesic

Uses

for the temporary relief of pain and itching associated with • minor burns • sunburn • minor cuts • scrapes • insect bites • minor skin irritations

Warnings

For external use only

Do not usein large quantities, particularly over raw surfaces or blistered areas

When using this productavoid contact with the eyes

Stop use and ask a doctor ifcondition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

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

Directions

• adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily • children under 2 years of age: ask a doctor

Other information

Store a room temperature • Protect from direct sunlight.

Inactive ingredients

Aloe Barbadensis Leaf Juice, Carbomer, Disodium EDTA, Ethylhexylglycerin, FD&C Blue NO.1, FD&C Yellow NO.5, Glycerin, Menthol, Maltodextrin, Propanediol, Polysorbate 20, Phenoxyethanol, Sodium Hydroxide, SD Alcohol, Water.

✓ Soothes & Cools Minor Burns

✓ Menthol Formula for Fast Pain Relief

✓ Helps Prevent Infection

PAIN RELIEVING GEL WITH ALOE

Mfd for and Distributed by:
Universal Distribution Center LLC
330 Applegarth Road, Monroe Township, NJ 08831
www.universaldc.com

MADE IN CHINA

Packaging

0.5% LIDOCAINE BURN RELIEF

0.5% LIDOCAINE BURN RELIEF 
lidocaine hydrochloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43473-099
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS0.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
GLYCERIN (UNII: PDC6A3C0OX)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
PROPANEDIOL (UNII: 5965N8W85T)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43473-099-083 in 1 BOX02/21/2026
1226 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01702/21/2026
Labeler - Nantong Health & Beyond Hygienic Products Inc. (421280161)
Establishment
NameAddressID/FEIBusiness Operations
Nantong Health & Beyond Hygienic Products Inc.421280161manufacture(43473-099)

Revised: 2/2026
Document Id: 4b636475-c805-0b73-e063-6394a90ac7c9
Set id: cf723c7b-495d-4bae-942c-561cf28af2d3
Version: 1
Effective Time: 20260221
 
Nantong Health & Beyond Hygienic Products Inc.