Witch Hazel by Cardinal Health (Leader) 70000 WITCH HAZEL liquid

Witch Hazel by

Drug Labeling and Warnings

Witch Hazel by is a Otc medication manufactured, distributed, or labeled by Cardinal Health (Leader) 70000. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Witch hazel, USP 86%

Purpose

Astringent

Uses

• for relief of minor skin irritations due to:
  • insect bites
  • minor cuts
  • minor scrapes

Warnings

For external use only.

• Avoid swallowing.

When using this product

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

condition worsens or symptoms persist for more than 7 days

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away..

Directions

apply to the affected area as often as necessary.

Other information

• keep tightly closed
• store at room temperature

Inactive ingredient

alcohol 14% by volume

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

Principal Display Panel

COMPARE TOT.N. DICKINSON'S® WITCH HAZEL active ingredient*

Witch Hazel

USP, 86% | Astringent

Alcohol 14% by Volume

Hamamelis Water

For relief of

Minor Skin Irritations

Due To:

Insect Bites

Minor Cuts

Minor Scrapes

FL OZ (mL)

*This product is not manufactured or distributed by Dickinson Brands, Inc., distributor of T.N. Dickinson's Witch Hazel.

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

DIST. BY

CAH DUBLIN, OH 43017

www.myleader.com

Package Label

LEADER Witch Hazel

INGREDIENTS AND APPEARANCE

WITCH HAZEL 
witch hazel liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70000-0615
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	842 mg  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70000-0615-1	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/30/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/30/2022

Labeler - Cardinal Health (Leader) 70000 (063997360)