Witch Hazel by Pharmacy Vlaue Alliance LLC / Vi-Jon, LLC WITCH HAZEL liquid

Witch Hazel by

Drug Labeling and Warnings

Witch Hazel by is a Otc medication manufactured, distributed, or labeled by Pharmacy Vlaue Alliance LLC, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Witch hazel 86%

Purpose

Astringent

use

for relief of minor skin irritations due to:

• insects bites
• minor cuts
• minor scrapes

Warnings

For external use only

When using this product

• avoid contact with the eyes

Stop use and ask a doctor if

• condition worsens or symptoms persist for more than 7 days

Keep out of reach of children

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

Directions

apply as often as needed

inactive ingredients

alcohol 14% by volume

Questions

Call 1-888-593-0593

disclaimer

This product is not manufactued or distributed by Dickinson Brand, Inc., distributorof T.N. Dickinson Witch Hazel.

If for any rason you are not satisfied with this product, please return it to the store where purchased for a full refund.

Adverse reactions

Distributed by: Phamacy Value Alliance LLC

407 East Lancaster Avenue, Wayne, PA 19087

www.emersongroup.com

Principal Display Panel

COMPARE TO

T.N.DICKINSON'S

Premier

Value

Witch

Hazel

u.s.p.

astringent

hamamelis water

for relief of minor skin

irritations due to:

• insects bites
• minor cuts
• minor scrapes

Square bottle uses less plastic

than a similarly sized round bottle

Recyclable ( if available in your area)

16 FL OZ

(1 PT) 473 mL

INGREDIENTS AND APPEARANCE

WITCH HAZEL 
witch hazel liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68016-822
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	842 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68016-822-43	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/15/2003

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	08/15/2003

Labeler - Pharmacy Vlaue Alliance LLC (101668460)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		790752542	manufacture(68016-822)