GOOD NEIGHBOR PHARMACY ALOE VERA- lidocaine hydrochloride gel 
Amerisourcebergen Drug Corporation

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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Good Neighbor Pharmacy Aloe Vera

Drug Facts

Active Ingredients

Lidocaine Hydrochloride 0.5%

Pain Reliever

Temporary relief of pain and itching due to sunburn, minor burns, insect bites, cuts, scrapes

For external use only

Do not use in large quantities, particularly over raw or blistered areas.

When using this product

• avoid contact with eyes.

Rinse with water if contact occurs.

Stop use and ask a doctor if

• condition worsens

or clear up and occur again within a few days.

• if symptoms persist for more than 7 days.

Keep out of reach of children.

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

• adults and children 2 years and older: apply to affected area not more than 3 - 4 times a day. • children under 2 years of age: consult a physician

Aloe Barbadensis Leaf Juice, Carbomer, Diazolidinyl Urea, Disodium EDTA, FD&C Blue #1, FD&C Yellow #5, Glycerin, Isopropyl Alcohol (0.05% v/v), Menthol, Polysorbate 80, Propylene Glycol, Triethanolamine, Water.

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 Aloe Vera Gel

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GOOD NEIGHBOR PHARMACY ALOE VERA 
lidocaine hydrochloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-083
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE500 g  in 100000 mg
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
MENTHOL (UNII: L7T10EIP3A)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24385-083-34500 mg in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34811/28/1988
Labeler - Amerisourcebergen Drug Corporation (007914906)
Establishment
NameAddressID/FEIBusiness Operations
Product Quest Mfg, LLC927768135manufacture(24385-083) , label(24385-083)

Revised: 7/2015
Document Id: 97a6327f-e5d9-4227-9f05-934b1f94d826
Set id: d94df507-99f1-4511-9ba8-7f63a38963b8
Version: 1
Effective Time: 20150722
 
Amerisourcebergen Drug Corporation