SUNBURN RELIEF- lidocaine hcl 0.5% gel 
Rite Aid

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

Use

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

*This product is not manufactured or distributed by Bayer

distributer of Solarcaine Cool Aloe Burn Relief Formula

DISTRIBUTED BY: RITE AID

30 HUNTER LANE

CAMP HILL, PA 17011

www.riteaid.com

SATISFACTION GUARANTEE:

If you're not satisfied,

we'll happily

refund your money.

Principal Panel Display

Compare to Salarcaine

Cool Aloe Burn Relief Formula

Pain Relieving Gel

with Lidocaine HCI*

SUNBURN

RELIEF 

PAIN RELIEVING GEL

WITH ALOE

Cool on contact

Great sunburn relief

Minor burn relief

NET WT 

8 OZ (226 g)

image description

SUNBURN RELIEF 
lidocaine hcl 0.5% gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0776
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS5 mg  in 1 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:11822-0776-3226 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/30/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34812/30/2019
Labeler - Rite Aid (014578892)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(11822-0776)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(11822-0776)

Revised: 10/2022
Document Id: 3e01f31a-3b76-4097-ba54-61cd2c62dc7c
Set id: b67af0c7-1ae8-4494-bb0e-d7f66ebca352
Version: 3
Effective Time: 20221003
 
Rite Aid