Witch Hazel by Meijer Distribution Inc Meijer Witch Hazel

Witch Hazel by

Drug Labeling and Warnings

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

Drug Details [pdf]

WITCH HAZEL- witch hazel spray spray 
Meijer Distribution Inc

----------

Meijer Witch Hazel

Active ingredient

Witch Hazel 86%

Purpose

Astringent

Uses

Relieves minor skin irritation due to:

• insect bites
• minor cuts
• minor scrapes

Warnings

For external use only.

Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120°F. Keep out of the reach of children. Use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

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
• 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 necessary
• to apply to face, moisten cotton ball or cleansing pad and gently wipe skin

Other information

store at room temperature

Inactive ingredient

alcohol (14%)

Questions?

Call 1-866-964-0939

Principal Display Panel

meijer

CONTINUOUS

witch

hazel

Astringent Spray

For Face and Body

Soothes irritated,

inflamed, oily, or

blemished skin

NET WT 6.0 0Z (170 g)

WITCH HAZEL 
witch hazel spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41250-383
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	146 g  in 170 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41250-383-06	170 g in 1 CAN; Type 0: Not a Combination Product	03/01/2021	05/31/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	03/01/2021	05/31/2025

Labeler - Meijer Distribution Inc (006959555)

Revised: 1/2026

Document Id: 48d54f7d-9c09-098a-e063-6394a90a7c88

34390-5

Set id: b364bf5b-e414-94f1-e053-2a95a90a5d6d

Version: 5

Effective Time: 20260120