TN DICKINSONS WITCH HAZEL ASTRINGENT- witch hazel liquid 
Dickinson Brands Inc.

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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Drug Facts

Active Ingredient:
All Natural Witch Hazel 100% (containing Alcohol 14%)

Purpose

Astringent

Uses:

Temporarily relieves minor skin irritations due to:

Warnings:

For external use only

When using this product avoid contact with eyes

Stop use and ask doctor if condition worsens or
symptoms persist for more than 7 days

Keep out of reach of children. If swallowed, get medical
help or contact Poison Control Center right away.

Directions:

Questions or Comments?
Call toll free: 1-888-860-2279
Dist. by: Dickinson Brands Inc.
East Hampton, CT 06424
MADE IN THE U.S.A.
www.tndickinsons.com
No animal testing

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

CLEANSE•SOOTHE•TREAT

#1
FIRST AID
ASTRINGENT
BRAND*

T.N.
DICKINSON'S®

Witch
hazel®

100% Natural Astringent

CLINICAL GRADE

Gentle Relief for
Oily, irritated, red,
damaged, blemished,
or inflamed skin

100% NATURAL
WITCH HAZEL

FOR FACE AND BODY

16 FL. OZ. (473 mL)

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label
TN DICKINSONS WITCH HAZEL ASTRINGENT 
witch hazel liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52651-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL86 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52651-001-06473 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product12/02/1989
2NDC:52651-001-05237 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product12/02/1989
3NDC:52651-001-0759 mL in 1 BOTTLE; Type 0: Not a Combination Product12/02/1989
4NDC:52651-001-043785 mL in 1 BOTTLE; Type 0: Not a Combination Product12/02/1989
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34712/02/1989
Labeler - Dickinson Brands Inc. (124620340)
Establishment
NameAddressID/FEIBusiness Operations
American Distilling Inc.065524738MANUFACTURE(52651-001) , API MANUFACTURE(52651-001)

Revised: 1/2023
Document Id: 84484184-24c7-43f4-aa4b-92719850355b
Set id: a9596cf1-8204-447d-90f6-622bf497a7e0
Version: 6
Effective Time: 20230105
 
Dickinson Brands Inc.