SKIN TONER- witch hazel liquid 
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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SKIN TONER 

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:

Aqua, Ethyl Alcohol, Aloe Barbadensis (Aloe Vera) Leaf Juice, Parfum

WITH ALOE VERA

SKIN CLEANSER

MAKE-UP REMOVER

AFTER SHAVING

For Face & Body

Clean | Soothe | Treat

Gentle Relief For 

Greasy, Rough, Injured, Inflamed, or Blemished Skin

NATURAL 100% 

WITH WITCH HAZEL (HAMAMEUS WATER)

Specifically formulated for purifying and conditioning of the skin.

Distributed by:

Universal Distribution Centre LLC

Edison, NJ 08817

www.universaldc.com

Made in Pakistan

Packaging

UToner1

SKIN TONER 
witch hazel liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-300
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL14 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52000-300-02473 mL in 1 BOTTLE; Type 0: Not a Combination Product12/29/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34712/29/2020
Labeler - Universal Distribution Center LLC (019180459)

Revised: 12/2020
Document Id: 01a8151a-436b-4638-aef0-c682117c5aae
Set id: b2ddc67d-c4bb-4227-af88-75c08135074b
Version: 1
Effective Time: 20201229
 
Universal Distribution Center LLC