WALG AFTRSN BURN RELIEF- lidocaine hydrochloride spray

WALG AFTRSN BURN RELIEF by

Drug Labeling and Warnings

WALG AFTRSN BURN RELIEF by is a Otc medication manufactured, distributed, or labeled by Walgreen Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Product

WALGREENS AFTERSUN BURN RELIEF SPRAY

Active Ingredients

Lidocaine Hydrochloride 0.5%

Purpose

Topical Anesthetic

Uses:

• Temporary relief of pain and itching
  
• Helps to relieve and soothe pain from sunburn, minor burns, skin irritations, scrapes, insect bites.

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:

• Adults and children 2 years or older: apply to affected area not more than 3-4 times daily.
  
• Children under 2 years of age: do not use; ask a doctor.

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)

INGREDIENTS AND APPEARANCE

WALG AFTRSN BURN RELIEF 
lidocaine hydrochloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-9919
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	0.5 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-9919-36	237 mg in 1 BOTTLE; Type 0: Not a Combination Product	11/30/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part348	11/30/2017

Labeler - Walgreen Company (008965063)

Registrant - Walgreen Company (008965063)