Natures Willow Itch Relief Lotion

Manufacturer
WB Ventures LLC
Effective date
2023-12-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:17:30

Label at a glance#

ProductNatures Willow Itch Relief
Active ingredientMENTHOL
Label structure9 sections

Indications and uses

For the temporary relief of pain and itching associated with: insect bites minor skin irritations scrapes sunburn

Dosage and administration

Adults and children over 2 years of age: apply to affected area not more than 3 times daily Children under 2 years of age: consult a physician

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.5%

Purpose

OTC - PURPOSE SECTION

External Analgeisc

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of pain and itching associated with:

  • insect bites
  • minor skin irritations
  • scrapes
  • sunburn

Warnings

WARNINGS SECTION

For external use only.

When using this product avoid contact with eyes.

Stop use and ask a doctor if

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children over 2 years of age: apply to affected area not more than 3 times daily
  • Children under 2 years of age: consult a physician

Inactive ingredients

INACTIVE INGREDIENT SECTION

1,2-Hexanediol, Camphor, Caprylhydroxamic Acid, Ceteareth-20, Cetearyl Alcohol, Cetyl Alcohol, Clary Oil, Eucalyptus Oil, Geranium Oil, Glyceryl Stearate, Helichrysum Gymnocephalum Oil, Jojoba Seed Oil, Lavender Oil, Propanediol, Sodium Hydroxide, Squalane, Stearic Acid, Stearyl Alcohol, Sunflower Seed Oil, Sweet Almond Oil, Water, White Willow Bark Extract

SPL Unclassified Section

DISTRIBUTED BY WB VENTURES LLC

COLD SPRING KY 41076

FOR MORE INFORMATION OR TO REPORT A SERIOUS ADVERSE EVENT CONTACT 1-888-609-4556

MADE IN CANADA

Package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73498-02473498-024-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

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
0ce01a78-6f33-501e-e063-6394a90a0589bdbd8880-5c53-211c-e053-2995a90a44322023-12-19WarningsExact identifier
spl id: 0ce01a78-6f33-501e-e063-6394a90a0589
spl set id: bdbd8880-5c53-211c-e053-2995a90a4432

Reported adverse events (FAERS/openFDA)#

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