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Witch Hazel by Chain Drug Consortium, LLC

Medically reviewed on October 26, 2017

Dosage form: liquid
Ingredients: WITCH HAZEL 842mg in 1mL
Labeler: Chain Drug Consortium, LLC
NDC Code: 68016-593

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.

Drug Facts

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

Principal Display Panel

Distilled extract of

Witch Hazel

Astringent

Alcohol 14% by volume

DISTRIBUTED BY: CHAIN DRUG CONSORTIUM, LLC.

3301 NW BOCA RATON BLVD, SUITE 101

BOCA RATON, FL 33431

PRODUCT OF USA

Questions or comments?

Call 1-877-753-3935

Monday-Friday 9AM-5PM EST

FL OZ (mL)

Package Label

Premier Value Witch Hazel Liquid

WITCH HAZEL 
witch hazel liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-593
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WITCH HAZEL (WITCH HAZEL) WITCH HAZEL842 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL 
Packaging
#Item CodePackage Description
1NDC:68016-593-16473 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34708/31/2014
Labeler - Chain Drug Consortium, LLC (101668460)

 
Chain Drug Consortium, LLC

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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