Drug Facts

Active ingredients	Purpose
Diphenhydramine hydrochloride 2%	Topical analgesic
Zinc acetate 0.1%	Skin protectant

Uses

temporarily relieves pain and itching due to:
- insect bites
- minor burns
- sunburn
- minor skin irritations
- minor cuts
- scrapes
- rashes due to poison ivy, poison oak, and poison sumac
dries the oozing and weeping of poison • ivy • oak • sumac

Warnings

For external use only.

Do not use

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

Ask a doctor before use

on chicken pox
on measles

When using this product do not get into eyes

Stop use and ask a doctor if

condition worsens
symptoms last 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 right away.

Directions

do not use more than directed
adults and children 2 years of age and older: spray on affected area not more than 3 to 4 times daily
children under 2 years of age: ask a doctor

Other Information

store at 20° C to 25° C (68° F to 77° F)

Inactive ingredients

glycerin, povidone, purified water, SD alcohol 40-B, trolamine

Distributed by:

SELECT BRAND DISTRIBUTORS

Pine Bluff, AR 71603 USA, AC(870) 535-3635

PRINCIPAL DISPLAY PANEL

FOR SKIN USE ONLY

select brand

Topical Analgesic

Skin Protectant

ITCH RELIEF SPRAY

*Compare to the active ingredients in

BENADRYL ITCH RELIEF SPRAY

EXTRA STRENGTH

Diphenhydramine HCl 2%

Zinc Acetate 0.1%

2 FL OZ (59 mL)

PDP

rear

SELECT BRAND ITCH RELIEF
diphenhydramine hydrochloride and zinc acetate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:15127-054
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	.2 g in 10 mL
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37)	ZINC ACETATE	.01 g in 10 mL

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
POVIDONES (UNII: FZ989GH94E)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:15127-054-02	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/03/2014

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part347	07/11/2012

Labeler - Select Brand (043562370)

Registrant - Weeks & Leo Co., Inc. (005290028)

Name	Address	ID/FEI	Business Operations
Establishment
Weeks & Leo Co., Inc.		005290028	manufacture(15127-054)

Select Brand Itch Relief Spray