UNIVERSAL WITCH HAZEL- witch hazel solution

Universal WITCH HAZEL by

Drug Labeling and Warnings

Universal WITCH HAZEL by is a Otc medication manufactured, distributed, or labeled by Universal Distribution Center LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients:

All natural distilled witch hazel 100%
(contains natural grain alcohol 14%)

Purpose

Astringent

Usage:

The soft toner is specifically developed to meet ultimate needs of purifying and conditioning for an array of skin types. It is a calm and non-drying formula which removes remaining traces of soap. It removes make-up or excess oils making your skin feeling soft, healthful, and smooth. It also smoothens the skin after shaving. Use as often as necessary. Apply directly from the bottle or dampen a cotton pad and smoothly wipe it off.

Warning:

For external use only. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

Keep out of reach of children.

Direction:

remove protective inner seal
 moisten cotton ball or cleansing pad and gently wipe skin
 apply as often as necessary

Ingredients:

Water, Hamamelis Virginiana (Witch Hazel) Leaf Water, Alcohol (14% by Volume), Benzyl Alcohol, Methylchloroisothiazolinone, methylisothiazolinone.

SPL UNCLASSIFIED SECTION

SKIN CLEANSER

MAKE-UP REMOVER

AFTER SHAVING

For Face & Body

Gentle Relief For

100% NATURAL ASTRINGENT

Specifically formulated for purifying and conditioning of the skin.

Distributed by:
Universal Distribution Center LLC
Edison, NJ 08817
www.universaldc.com

This Product is Not Tested on Animals 

Made in Jordan

Packaging

INGREDIENTS AND APPEARANCE

UNIVERSAL WITCH HAZEL 
witch hazel solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-414
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HAMAMELIS VIRGINIANA LEAF WATER (UNII: 8FP93ED6H2)
ALCOHOL (UNII: 3K9958V90M)
BENZYL ALCOHOL (UNII: LKG8494WBH)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-414-06	177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	07/01/2023

Labeler - Universal Distribution Center LLC (019180459)