SUNBURN RELIEF- lidocaine hcl 0.5% gel 
WALMART INC.

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.

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Sunburn Relief Gel
005.002/005AC-AD

Active ingredient

Lidocaine HCl 0.5%

Purpose

External analgesic

Uses

for the temporary relief of pain and itching associated with

Warnings

For external use only

Do not use

in large quantities, particularly over raw surfaces or blistered areas

When using this product

avoid contact with the eyes

Stop use and ask a doctor if

condition 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

Inactive ingredients

water, propylene glycol, glycerin, Aloe barbadensis leaf juice, triethanolamine, isopropyl alcohol, polysorbate 80, carbomer, phenoxyethanol, benzyl alcohol, menthol, disodium EDTA, blue 1, yellow 5

Questions?  1-888-287-1915

DISTRIBUTED BY Walmart Inc., Bentonville, AR 72716

*This product is not manufactured or distributed by Bayer Healthcare,

LLC, owner of the registered trademark Solarcaine

Cool Aloe Burn Relief Formula.

Satisfaction guaranteed - For questions or comments please call 1-888-287-1915

Principal Display Panel

NDC 79903-037-34

EquateTM

Compare to Solarcaine Cool Aloe Burn Relief Formula active ingredient*

Burn

Relief Gel

WITH LIDOCAINE

Pain Relieving Gel

with Aloe

Empty & Replace Cap

PLASTIC BOTTLE

how2recycle.info

Relief from:

Moisturizer

NET WT 8 OZ (226g)

image description

SUNBURN RELIEF 
lidocaine hcl 0.5% gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-037
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
water (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
TROLAMINE (UNII: 9O3K93S3TK)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
MENTHOL (UNII: L7T10EIP3A)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79903-037-34226 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/23/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34812/23/2020
Labeler - WALMART INC. (051957769)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(79903-037)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(79903-037)

Revised: 10/2022
Document Id: eb2a46e0-74ec-4ed5-a383-d0a3a0fb73c7
Set id: 1eef58d3-7671-48f6-b4c4-4b83eae9d197
Version: 5
Effective Time: 20221004
 
WALMART INC.