GOOD NEIGHBOR PHARMACY BURN RELIEF ALOE EXTRA- lidocaine spray

Good Neighbor Pharmacy Burn Relief by

Drug Labeling and Warnings

Good Neighbor Pharmacy Burn Relief by is a Otc medication manufactured, distributed, or labeled by AmerisourceBergen Drug Corporation, Product Quest Mfg, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Lidocaine 0.50%

Purpose

External analgesic

Uses

Temporarily relieves pain and itching due to: sunburn minor

burns minor cuts scrapes insect bites minor skin irritations

Warnings

For external use only.

Flammable: Do not use while smoking or near heat or flame

Do not use

in large quantities, particularly over raw surfaces or blistered areas

When using this product

keep out of eyes use only as directed.

do not puncture or incinerate. Contents under pressure. Do not store at

temperatures above 120ºF.

Stop use and ask doctor if

Condition worsens 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.

Directions

shake well 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 to apply to face, spray into palm of

hand and gently apply

Inactive ingredients

Aloe Barbadensis Leaf Juice,

SD Alcohol 40, Propylene Glycol, Glycerin, Simethicone, Tocopheryl

Acetate, Triethanolamine, Carbomer, Diazolidinyl Urea, Methylparaben,

Propylparaben, Disodium Cocoamphodipropionate, Disodium EDTA.

*This product is not manufactured or distributed by Schering-Plough Healthcare Products, Inc., owner of the Solarcaine® trademark. Distributed By AmerisourceBergen 1300 Morris Drive, Chesterbrook, PA 19087 Visit us at www.goodneighborpharmacy.com

Good Neighbor Pharmacy Burn Relief Spray

INGREDIENTS AND APPEARANCE

GOOD NEIGHBOR PHARMACY BURN RELIEF  ALOE EXTRA
lidocaine spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 46122-113
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	.50 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALCOHOL (UNII: 3K9958V90M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
SIMETONE (UNII: 387DQL493M)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
DISODIUM COCOAMPHODIPROPIONATE (UNII: 6K8PRP397M)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 46122-113-21	127 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/28/2011

Labeler - AmerisourceBergen Drug Corporation (007914906)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg, LLC		927768135	manufacture(46122-113) , label(46122-113)