Witch Hazel by Walgreens WITCH HAZEL liquid

Witch Hazel by

Drug Labeling and Warnings

Witch Hazel by is a Otc medication manufactured, distributed, or labeled by Walgreens. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Witch Hazel 86%

Purpose

Astringent

Uses

for relief of minor skin irritations due to:

• insect bites
• minor cuts
• minor scrapes

Warnings

• For external use only
• Avoid swallowing.

When using this product

• avoid contact with the eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

condition worsens or symptoms persist for more than 7 days.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

apply to the affected area as often as necessary.

Other information

• keep tightly closed.
• store at room temperature

Inactive ingredient

alcohol 14% by volume

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST 

Principal Display Panel

Astringent

Witch Hazel

For Face & Body

Gentle relief for:

• Oily, irritated, red, damaged, blemished or inflamed skin
• Skin irritations due to insect bites, minor cuts or minor scrape
• Alcohol 14% by volume

FL OZ (mL)

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

walgreens.com

MADE IN U.S.A

Package Label

Well at Walgreens Witch Hazel

INGREDIENTS AND APPEARANCE

WITCH HAZEL 
witch hazel liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0039
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: 0363-0039-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/31/2014	12/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part347	07/31/2014	12/30/2020

Labeler - Walgreens (008965063)