Witch Hazel by Rite Aid Corporation Drug Facts

Witch Hazel by

Drug Labeling and Warnings

Witch Hazel by is a Otc medication manufactured, distributed, or labeled by Rite Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WITCH HAZEL- witch hazel liquid 
Rite Aid Corporation

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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 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

Principal Display Panel

astringent

WITCH HAZEL

ALCOHOL 14% BY VOLUME

HAMAMELIS WATER

For relief of minor skin irritations due to insect bites:

•  Minor cuts 
• Minor scrapes

FL OZ (mL)

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

DISTRIBUTED BY:

RITE AID, 30 HUNTER LANE,

CAMP HILL, PA 17011

www.riteaid.com

Package Label

RITE AID Witch Hazel

RITE AID Witch Hazel

WITCH HAZEL 
witch hazel liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-3689
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: 11822-3689-3	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/03/2022	02/28/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	01/03/2022	02/28/2026

Labeler - Rite Aid Corporation (014578892)

Revised: 1/2026

Document Id: cb32c855-6a0e-4a59-aebc-f56989bfcaa8

34390-5

Set id: eb0a4d29-bbfa-4cb8-a7ad-c953e0fdfb03

Version: 5

Effective Time: 20260102