WALGREENS SUNBURN RELIEF- lidocaine gel 
WALGREEN COMPANY

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.

----------

Walgreens Sunburn Relief Gel

Active ingredient

Lidocaine 0.8% (as Lidocaine HCI)

Purpose

External Analgesic

Uses

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

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 eyes. If contact occurs, rinse with water to remove.

Stop use and ask a doctor if

• condition worsens • symptoms persist for more than 7 days • symptoms clear up and occur again within a few days

Keep out of reach of children

If swallowed, seek medical help or contact a Poison Control Center immediately.

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.

Inactive ingredients

water, aloe barbadensis leaf juice, alcohol denat., propylene glycol, laureth-23, glycerin, polysorbate 20, allantoin, carbomer, triethanolamine, menthyl lactate, disodium EDTA, menthol, aleurites moluccanus seed extract, carica papaya (papaya) fruit extract, colocasia antiquorum root extract, mangifera indica (mango) fruit extract, passiflora incarnata flower extract, plumeria acutifolia flower extract, psidium guajava fruit extract, tocopheryl acetate, tocopherol, phenoxyethanol, benzyl alcohol, fragrance, blue 1.

W97751E&F1

WALGREENS SUNBURN RELIEF 
lidocaine gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0985
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE8 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
MANGO (UNII: I629I3NR86)  
ALCOHOL (UNII: 3K9958V90M)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
LAURETH-23 (UNII: N72LMW566G)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
ALLANTOIN (UNII: 344S277G0Z)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
TROLAMINE (UNII: 9O3K93S3TK)  
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
LEVOMENTHOL (UNII: BZ1R15MTK7)  
KUKUI NUT OIL (UNII: TP11QR7B8R)  
PAPAYA (UNII: KU94FIY6JB)  
COLOCASIA ESCULENTA ROOT (UNII: H7B71Q0G0D)  
PASSIFLORA INCARNATA FLOWER (UNII: K8F3G29S6Z)  
GUAVA (UNII: 74O70D6VG0)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
PLUMERIA ALBA FLOWER OIL (UNII: T69Z2432CU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0985-68453 g in 1 BOTTLE; Type 0: Not a Combination Product11/08/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34810/03/2017
Labeler - WALGREEN COMPANY (008965063)

Revised: 1/2022
Document Id: d506e2b2-5396-043d-e053-2995a90ae77e
Set id: d5067903-c559-dc6d-e053-2995a90a8ee3
Version: 2
Effective Time: 20220107
 
WALGREEN COMPANY