Witch Hazel by Premier Brands of America Inc. WITCH HAZEL spray

Witch Hazel by

Drug Labeling and Warnings

Witch Hazel by is a Otc medication manufactured, distributed, or labeled by Premier Brands of America Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

Flammable:

Keep away from heat, sparks, and open flame. Contents under pressure. Do not puncture or incinerate. Do not store at a temperature above 120°F.

When using this product

• avoid spraying in the eyes. If contact occurs rinse thoroughly with water.
• use only as directed.
• intentional misuse by deliberately concentrating and inhaling the contents can be harful or fatal.

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 needed
• 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

premier

solutions

WITCH

HAZEL

CONTINUOUS SPRAY

WITCH HAZEL 86%/

ASTRINGENT

NATURAL ASTRINGENT

FOR FACE & BODY

Cleanses & soothes

irritated,inflamed, oily,

or blemished skin

NET WT. 6.0 0Z. (170 g)

INGREDIENTS AND APPEARANCE

WITCH HAZEL 
witch hazel spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 56104-904
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	860 mg  in 1 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 56104-904-01	170 g in 1 CAN; Type 0: Not a Combination Product	06/23/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/27/2023

Labeler - Premier Brands of America Inc. (063849780)