WALG AFTRSN BURN RELIEF- lidocaine hydrochloride spray 
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.

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WAG Aftrsn Burn Relief Spray 8oz

Product

WALGREENS AFTERSUN BURN RELIEF SPRAY

Active Ingredients

Lidocaine Hydrochloride 0.5%

Purpose

Topical Anesthetic

Uses:

Warnings:

For external use only

Do not use

in large quantities, particularly over raw surfaces or areas with blisters.

When using this product:

  • Avoid contact with eyes.

Stop use and ask a doctor if:

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

Inactive Ingredients

Deionized Water, Glycerin, Propanediol, Aloe Barbadensis Leaf Juice, Carbomer, Tocopherol Acetate, PEG-40 Hydrogenated Castor Oil, Sodium Lauroyl Sarcosinate, Disodium EDTA, Phenoxyethanol, Sodium Hydroxide

Questions or comments?

www.walgreens.com or call toll free 1-800-XXX-XXXX

PRINCIPAL DISPLAY PANEL

Walgreens
Sunburn Relief
CONTINUOUS SPRAY
LIDOCAINE 0.5% /
EXTERNAL ANALGESIC
PAIN RELIEF
LIDOCAINE
8 OZ (227 g)

Walgreens
Sunburn Relief
CONTINUOUS SPRAY
LIDOCAINE 0.5% /
EXTERNAL ANALGESIC
PAIN RELIEF
LIDOCAINE
8 OZ (227 g)

WALG AFTRSN BURN RELIEF 
lidocaine hydrochloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9919
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS0.5 mg  in 100 mg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-9919-36237 mg in 1 BOTTLE; Type 0: Not a Combination Product11/30/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34811/30/2017
Labeler - Walgreen Company (008965063)
Registrant - Walgreen Company (008965063)

Revised: 10/2017
Document Id: e8dd78fa-e537-4523-833d-21d554912d4a
Set id: de3e40b5-0c2d-45d6-a8fb-17e9a1041c0e
Version: 2
Effective Time: 20171005
 
Walgreen Company