Natures Willow Itch Relief Lotion

Natures Willow Itch Relief by

Drug Labeling and Warnings

Natures Willow Itch Relief by is a Otc medication manufactured, distributed, or labeled by WB Ventures LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NATURES WILLOW ITCH RELIEF- menthol lotion 
WB Ventures LLC

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Natures Willow Itch Relief Lotion

Active ingredient

Menthol 0.5%

Purpose

External Analgeisc

Uses

For the temporary relief of pain and itching associated with:

• insect bites
• minor skin irritations
• scrapes
• sunburn

Warnings

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

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

Directions

• 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

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

NATURES WILLOW ITCH RELIEF 
menthol lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73498-024
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
JOJOBA OIL (UNII: 724GKU717M)
EUCALYPTUS OIL (UNII: 2R04ONI662)
HELICHRYSUM GYMNOCEPHALUM WHOLE (UNII: 0369G6I64W)
ALMOND OIL (UNII: 66YXD4DKO9)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
WATER (UNII: 059QF0KO0R)
SALIX ALBA BARK (UNII: 205MXS71H7)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SUNFLOWER OIL (UNII: 3W1JG795YI)
LAVENDER OIL (UNII: ZBP1YXW0H8)
PROPANEDIOL (UNII: 5965N8W85T)
STEARIC ACID (UNII: 4ELV7Z65AP)
CLARY SAGE OIL (UNII: 87L0D4U3M0)
SQUALANE (UNII: GW89575KF9)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETYL ALCOHOL (UNII: 936JST6JCN)
PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73498-024-01	226 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/20/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/30/2021	06/30/2024

Labeler - WB Ventures LLC (067482664)

Revised: 12/2023

Document Id: 0ce01a78-6f33-501e-e063-6394a90a0589

34390-5

Set id: bdbd8880-5c53-211c-e053-2995a90a4432

Version: 3

Effective Time: 20231219