Natures Willow Bug Bite Patch

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 Bug Bite Patch
Active ingredientCALENDULA OFFICINALIS FLOWER, SALIX ALBA BARK
Label structure11 sections

Indications and uses

Uses* For the temporary relief of symptoms associated with insect bites.

Dosage and administration

Adults and children over 12 years of age: 1. Clean and dry the affected area. 2. Peel off a patch from the transparent backing. 3. Apply carefully on the affeced area. To prevent touching the patch with your fingers, use the side tab. 4. Keep the patch on until the nuisance is gone. Do not exceed 8 hours of application. Children under 12 years of age: consult a physician

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Calendula Officinalis Flower Extract 0.002 mg

Salix Alba (Willow) Bark Extract 0.004 mg

Purpose

OTC - PURPOSE SECTION

Purpose*

Calendula Officinalis Flower Extract 0.002 mg

Reduces scarring, speeds healing
Salix Alba (Willow) Bark Extract 0.004 mgTopical analgesic

Uses

INDICATIONS & USAGE SECTION

Uses*

For the temporary relief of symptoms associated with insect bites.

Warnings

WARNINGS SECTION

For external use only. Avoid contact with eyes, mucous membranes, damaged skin or wounds.

Do not use if you are allergic to any ingredients in this product or by persons with known sensitivity to aspirin.

Stop use and ask a doctor if symptoms worsen or persist for more than 7 days.

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

Discontinue treatment in case of skin irritation, redness or rash occurs.

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 Poision Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12 years of age:

1. Clean and dry the affected area.

2. Peel off a patch from the transparent backing.

3. Apply carefully on the affeced area. To prevent touching the patch with your fingers, use the side tab.

4. Keep the patch on until the nuisance is gone. Do not exceed 8 hours of application.

Children under 12 years of age: consult a physician

Other information

OTHER SAFETY INFORMATION

Damaged packaging could compromise the operation and safety of the product.

  • Do not use if packaging is broken or punctured.
  • Disposable Single Use.
  • Store in cool, dry place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates Copolymer, Eucalyptus Globulus Leaf Oil, Glycine Soja Oil, Helichrysum Italicum Flower Extract, Lavandula Angustifolia Oil, Limonene, Linalool, Linseed Acid, Mentha Piperita (Peppermint) Oil, Menthol, Oleyl Alcohol, Pelargonium Graveolens Oil, Propylene Glycol, Tocopheryl Acetate, Vitis Vinifera Seed Oil, Zanthoxylum Bungeanum Fruit Extract

Questions or comments?

OTC - QUESTIONS SECTION

Questions or comments?1-888-609-4556

SPL Unclassified Section

*This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box LabelBox Label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73498-02573498-025-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
0cdee317-4b8a-be0a-e063-6394a90abc6bca677ffa-5730-7956-e053-2995a90a3dea2023-12-19WarningsExact identifier
spl id: 0cdee317-4b8a-be0a-e063-6394a90abc6b
spl set id: ca677ffa-5730-7956-e053-2995a90a3dea

Reported adverse events (FAERS/openFDA)#

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