UNIVERSAL WITCH HAZEL- witch hazel solution 
Universal Distribution Center LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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WITCH HAZEL SOLUTION

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.

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

WitchHazel-414

UNIVERSAL WITCH HAZEL 
witch hazel solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-414
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
HAMAMELIS VIRGINIANA LEAF WATER (UNII: 8FP93ED6H2)  
ALCOHOL (UNII: 3K9958V90M)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52000-414-06177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34707/01/2023
Labeler - Universal Distribution Center LLC (019180459)

Revised: 7/2023
Document Id: 185481dd-ffd6-49f8-8419-3b7c7451e3d2
Set id: 7e0b56ef-fa41-4862-b387-5b58d81d67d4
Version: 1
Effective Time: 20230707
 
Universal Distribution Center LLC