Witch Hazel by Good Sense (Geiss, Destin & Dunn, Inc.) WITCH HAZEL liquid

Witch Hazel by

Drug Labeling and Warnings

Witch Hazel by is a Otc medication manufactured, distributed, or labeled by Good Sense (Geiss, Destin & Dunn, Inc.). Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Witch hazel 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 the 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

Witch Hazel USP

Alcohol 14% by Volume

Astringent

Hamamelis Water

For relief of minor skin irritations due to:

• Insect Bites
• Minor Cuts
• Minor Scrapes

FL OZ (mL)

Compare to active ingredient of T.N. Dickinson's® Witch Hazel*

*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.

Distributed by: Geiss, Destin & Dunn, Inc.

Peachtree City, GA 30269

www.valuelabels.com

Package Label

GOODSENSE Witch Hazel USP

INGREDIENTS AND APPEARANCE

WITCH HAZEL 
witch hazel liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50804-390
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: 50804-390-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/30/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part347	09/30/2016

Labeler - Good Sense (Geiss, Destin & Dunn, Inc.) (076059836)