GOOD NEIGHBOR PHARMACY ITCH RELIEF EXTRA STRENGTH- diphenhydramine, zinc acetate aerosol, spray 
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 Itch Relief

Drug Facts

Active ingredients

Purpose

Uses

Temporarily relieves pain and itching associated with: • insect bites • minor

burns • sunburn • minor cuts • scrapes • minor skin irritations • rashes due to poison

ivy, oak and sumac • dries the oozing and weeping of poison ivy, oak and sumac

Warnings

For external use only.

Flammable:

Do not use while smoking or near heat or flame

Do not use

on large areas of the body • with any other product containing diphenhydramine, even one taken by mouth

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.

Ask a doctor before use

• on chicken pox • on measles

Stop use and ask doctor if

• condition worsens • symptoms last more than 7 days

• symptoms clear up and occur again in 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

Alcohol Denat., Glycerin, PVP, Tromethamine, Water.

*This product is not manufactured or distributed

by McNeil Consumer Healthcare, owner and

distributor of the Benadryl® trademark.

Distributed By AmerisourceBergen

1300 Morris Drive, Chesterbrook, PA 19087

Visit us at www.goodneighborpharmacy.com

Good Neighbor Pharmacy Itch Relief

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GOOD NEIGHBOR PHARMACY ITCH RELIEF  EXTRA STRENGTH
diphenhydramine, zinc acetate aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-114
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE2 g  in 100 g
Zinc Acetate (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
PVP/VA COPOLYMER (UNII: D9C330MD8B)  
TROMETHAMINE (UNII: 023C2WHX2V)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:46122-114-2185 g in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34810/28/2011
Labeler - AmerisourceBergen Drug Corporation (007914906)
Establishment
NameAddressID/FEIBusiness Operations
Product Quest Mfg, LLC927768135manufacture(46122-114) , label(46122-114)

Revised: 9/2015
Document Id: ad9688ce-79d1-44ec-aeaf-a7c9e6c7f2fe
Set id: 4775e0b1-3841-401e-8c4f-15b7536e46a0
Version: 1
Effective Time: 20150908
 
AmerisourceBergen Drug Corporation