Humco Witch Hazel

Manufacturer
Humco Holding Group, Inc. | Pharma Nobis, LLC
Effective date
2023-12-15
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:04:34

Label at a glance#

ProductHumco Witch Hazel
Active ingredientWITCH HAZEL
Label structure10 sections

Dosage and administration

Apply liberally to the affected area as often as necessary.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Wicth Hazel

Purpose

OTC - PURPOSE SECTION

Astringent

Use

INDICATIONS & USAGE SECTION

For relief of minor skin irritations due to:

  • Minor cuts
  • scrapes
  • burns
  • insect bites

Warnings

WARNINGS SECTION

For external use only.

  • avoid contact with eyes.

When using this product stop use and consult a doctor if:

OTC - STOP USE SECTION

  • condition persists or gets worse.
  • symptoms do not improve in 7 days.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately. In case of eye contact, flush eyes with running water for 15 minutes.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally to the affected area as often as necessary.

Inactive ingredents

INACTIVE INGREDIENT SECTION

Alcohol 14% and purified water.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

witchwitch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0395-3213-16Humco Witch Hazel473 mL in 1 BOTTLELIQUID4735

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0395-3213HUMCO WITCH HAZEL (WITCH HAZEL) LIQUID [HUMCO HOLDING GROUP, INC.]5Current NDC, Legacy NDC, 1 package rows20231216_3cf07016-a129-49ca-8fad-b67dda5aa009.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0395-32130395-3213-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
WITCH HAZEL101I4J0U34ACTIB

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
Humco Witch HazelWITCH HAZELHumco Holding Group, Inc.3cf07016-a129-49ca-8fad-b67dda5aa0092023-12-15WarningsExact identifier
ndc (package): 0395-3213-16
ndc (product): 0395-3213
ndc11 (package): 00395321316
spl id: 0c936cb3-838f-0603-e063-6394a90a0640
spl set id: 3cf07016-a129-49ca-8fad-b67dda5aa009

Reported adverse events (FAERS/openFDA)#

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