84558-016

Manufacturer
GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd
Effective date
2026-06-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-06-16 05:10:16

Label at a glance#

ProductSEEBEELLAR TOLNAFTATE 1% ANTIFUNGAL BODY WASH
Active ingredientTOLNAFTATE
Label structure12 sections

Dosage and administration

1. Use daily during shower or bath 2. Wet skin thoroughly, lather into foam, apply to affected areas, and massage gently 3. Leave foam on skin for 1-2 minutes, then rinse thoroughly 4. For best results, use consistently every day

Storage and handling

Store at room temperature(15°-30°C /59°-86°F) Protect from excessive heat and direct sunlight

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1% (w/w)

Purpose

OTC - PURPOSE SECTION

Antifungal

Use

INDICATIONS & USAGE SECTION

1. For the treatment and prevention of common fungal skin
infections (athlete's foot, ringworm, jock itch, and tinea
versicolor) when used as part of your daily shower routine.
2. Temporarily relieves itching, scaling, burning, redness, and
discomfort associated with these fungal conditions, including
tinea versicolor.
2. Cleanses skin thoroughly while delivering antifungal benefits.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

Do not use on scalp or mucous membranes (eyes, nose, mouth, genital areas). If contact with eyes occurs, rinse
thoroughly with water.

Do not use on children under 2 years of age unless directed by a doctor.
If pregnant or breastfeeding, consult a healthcare professional before use.
Do not use if you areallergic to any ingredient in this product.

OTC - WHEN USING SECTION

·Avoid contact with eyes
·If irritation occurs, please stop using

OTC - STOP USE SECTION

- Irritation, redness, or rash develops or worsens.
- No improvement in symptoms after 4 weeks for athlete's foot, ringworm, or tinea versicolor, or after 2 weeks for jock itch.
- The infection spreads or becomes severe.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

1. Use daily during shower or bath
2. Wet skin thoroughly, lather into foam, apply to affected areas, and massage gently
3. Leave foam on skin for 1-2 minutes, then rinse thoroughly
4. For best results, use consistently every day

Other information

STORAGE AND HANDLING SECTION

Store at room temperature(15°-30°C /59°-86°F)
Protect from excessive heat and direct sunlight

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Sodium Lauroyl Sarcosinate,Cocamidopropyl Betaine,
Lauryl Glucoside, Disodium Cocoyl Glutamate,Glycerin, Sodium
Lauroamphoacetate,Trehalose,Panthenol, Hamamelis Virginiana
Water, Phenoxyethanol, Aloe Barbadensis Extract, Sodium
Chloride, Hydrolyzed Sodium Hyaluronate, Hydrolyzed Oats,
Allantoin, Sodium Benzoate, Menthol, Arginine,Melaleuca
Alternifolia (Tea Tree) Leaf Oil, Mentha Arvensis Extract,Citric
Acid, Fragrance, Disodium Edta

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84558-01684558-016-01, 84558-016-02, 84558-016-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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
SEEBEELLAR TOLNAFTATE 1% ANTIFUNGAL BODY WASHSEEBEELLAR TOLNAFTATE 1% ANTIFUNGAL BODY WASHGUANGZHOU YUSONG FINE CHEMICLS Co., Ltd54050e6b-a7f1-5067-e063-6394a90aebe52026-06-11WarningsExact identifier
ndc (package): 84558-016-02
ndc (package): 84558-016-01
ndc (package): 84558-016-03
ndc (product): 84558-016
ndc11 (package): 84558001602
ndc11 (package): 84558001601
ndc11 (package): 84558001603
spl id: 54051812-504a-da1d-e063-6294a90adbe1
spl set id: 54050e6b-a7f1-5067-e063-6394a90aebe5

Reported adverse events (FAERS/openFDA)#

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