Lavinso Athlete’s Foot Antifungal Spray – Labeling

Manufacturer
Lavinso Trading LLC | AARNAV GLOBAL EXPORTS
Effective date
2025-09-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:14:33

Label at a glance#

ProductLavinso Athlete Foot
Active ingredientTOLNAFTATE
Label structure14 sections

Storage and handling

Other information • Store at 59–86 °F (15–30 °C) • Safety sealed: do not use if shrink-band around cap is broken or missing

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient
Tolnaftate 1%

OTC - PURPOSE SECTION

Purpose
Antifungal

INDICATIONS & USAGE SECTION

Uses
• Cures most athlete’s foot (tinea pedis) and jock itch (tinea cruris)
• Helps prevent most athlete’s foot with daily use
• Relieves itching, burning, cracking and scaling associated with these conditions

WARNINGS SECTION

Warnings
For external use only

OTC - DO NOT USE SECTION

Do not use
• On children under 2 years of age unless directed by a doctor

OTC - WHEN USING SECTION

When using this product
• Avoid contact with eyes
• Use only as directed

OTC - STOP USE SECTION

Stop use and ask a doctor if
• Irritation occurs
• There is no improvement within 4 weeks (athlete’s foot) or 2 weeks (jock itch)

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.

INSTRUCTIONS FOR USE SECTION

Directions
• Clean and dry the affected area
• Shake well before use. Spray a thin layer twice daily (morning and night)
• For athlete’s foot, pay special attention to spaces between the toes
• Use daily for 4 weeks for athlete’s foot; 2 weeks for jock itch
• To help prevent athlete’s foot, apply once daily
• Keep feet dry; change socks daily. Supervise children in use
• Not effective on scalp or nails

STORAGE AND HANDLING SECTION

Other information
• Store at 59–86 °F (15–30 °C)
• Safety sealed: do not use if shrink-band around cap is broken or missing

INACTIVE INGREDIENT SECTION

Inactive ingredients
Aloe Barbadensis Leaf Juice, Citric Acid, Denatured Alcohol 40-B, Ethylhexylglycerin, Eucalyptus Globulus Leaf Oil, Lavender Oil, Menthol, PEG-40 Hydrogenated Castor Oil, Peppermint Oil, Phenoxyethanol, Propylene Glycol, Purified Water, Sodium Citrate, Tea Tree Leaf Oil.

OTC - QUESTIONS SECTION

Questions?
Email us at info@lavinso.com or visit lavinso.com

When using this product

DOSAGE & ADMINISTRATION SECTION

• Avoid contact with eyes
• Use only as directed

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ATHLETE’S FOOT
ANTIFUNGAL SPRAY
Tolnaftate 1%
Cures & prevents most athlete’s foot
Fast-dry, cooling botanical formula
118 ML / 4.0 FL OZ

Designed in USA
Distributed by
Lavinso Trading LLC
300 Sunny Isles Blvd, Unit 1204
Sunny Isles Beach, FL 33160 USA

Made in India
NDC 87011-101
Batch No
Exp Date

BoxBox

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
313421tolnaftate 1 % Topical SprayPSN3
313421tolnaftate 10 MG/ML Topical SpraySCD3
313421tolnaftate 1 % Topical SpraySY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87011-101-01Lavinso Athlete Foot118 mL in 1 BOTTLE, SPRAYSPRAY1183
87011-101-02Lavinso Athlete Foot1 in 1 BOXSPRAY13

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87011-10187011-101-01, 87011-101-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
3f780893-3e37-8648-e063-6294a90ab9f23cb9f025-79bf-7422-e063-6294a90ae6092025-09-23WarningsExact identifier
spl id: 3f780893-3e37-8648-e063-6294a90ab9f2
spl set id: 3cb9f025-79bf-7422-e063-6294a90ae609

Reported adverse events (FAERS/openFDA)#

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