Witch Hazel

Manufacturer
Harris Teeter, LLC
Effective date
2023-02-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:36:51

Label at a glance#

ProductWitch Hazel
Active ingredientWITCH HAZEL
Label structure10 sections

Indications and uses

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

Dosage and administration

apply to the affected area as often as necessary.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Witch hazel 86%

Purpose

OTC - PURPOSE SECTION

Astringent

Uses

INDICATIONS & USAGE SECTION

for relief of minor skin irritations due to:

  • insect bites
  • minor cuts
  • minor scrapes

Warnings

WARNINGS SECTION

For external use only.

Avoid swallowing.

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens or symptoms persist for more than 7 days.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

apply to the affected area as often as necessary.

Other information

SPL UNCLASSIFIED SECTION

  • keep tightly closed
  • store at room temperature

Inactive ingredient

INACTIVE INGREDIENT SECTION

alcohol 14% by volume

Questions or comments?

OTC - QUESTIONS SECTION

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

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WITCH HAZEL

Alcohol 14% by volume

Astrigent

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 UNDER CAP IS BROKEN OR MISSING.

PROUDLY DISTRIBUTED BY:

hARRIS TEETER, LLC

MATTHEWS, INC 28105

1-800-432-6111 or harristeeter.com

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HARRIS TEETER Witch Hazel
HARRIS TEETER Witch Hazel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69256-390-162023-02-11C16284748780-1f386c64a-45dc-0266-e053-dadaa90a7c1aDrug Facts
69256-390-162023-01-30C16284748780-1f386c64a-45dc-0266-e053-dadaa90a7c1aDrug Facts

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69256-39069256-390-16

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WITCH HAZEL101I4J0U34ACTIB
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
56ec5186-89c4-4d32-b974-3537e6e4bbb5d5ddce8b-1e22-4fc9-ab9f-d8873de601c02025-07-11WarningsExact identifier
spl set id: d5ddce8b-1e22-4fc9-ab9f-d8873de601c0

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.