Witch Hazel

Manufacturer
Cardinal Health (Leader) 70000
Effective date
2025-02-04
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:54:23

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, USP 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 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

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LEADER Witch Hazel
LEADER Witch Hazel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70000-0615-1Witch Hazel473 mL in 1 BOTTLE, PLASTICLIQUID4735

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70000-0615WITCH HAZEL LIQUID [CARDINAL HEALTH (LEADER) 70000]5Current NDC, Legacy NDC, 1 package rows20250206_36deb7de-14b0-44a4-89bb-51cc1770e65b.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70000-0615-1ML - Milliliter70000-0615e682b680-1366-47fa-849a-17a7af677f1012023-06-06

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
70000-061570000-0615-1

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
Witch HazelWITCH HAZELCardinal Health (Leader) 7000036deb7de-14b0-44a4-89bb-51cc1770e65b2025-02-04WarningsExact identifier
ndc (package): 70000-0615-1
ndc (product): 70000-0615
ndc11 (package): 70000061501
spl id: 6729dd63-130c-4c96-8ade-ff3beb58f841
spl set id: 36deb7de-14b0-44a4-89bb-51cc1770e65b

Reported adverse events (FAERS/openFDA)#

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