VXGXO ANTIFUNGAL SOAP WITH TEA TREE OIL

Manufacturer
Guangdong Aimu Biological Technology Co., Ltd
Effective date
2026-08-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-18 02:02:03

Label at a glance#

ProductVXGXO antifungal with tea tree oil
Active ingredientTOLNAFTATE
Label structure11 sections

Indications and uses

1.For effective treatment of most athlete's foot (tinea pedis), ringworm (tineacorporis)and jock itch (tinea cruris). 2.For effective relief of itching, burning, and cracking skin. 3.For the prevention of most athlete's foot (tinea pedis) with daily use.

Dosage and administration

Wash he affected area and dry thoroughly. Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor Supervise children in the use of this product. For athlete's foot: pay special attention to spaces between the toes; wear wellfitting, ventilated shoes, and change shoes and socks at least once daily. For athlete's foot and ringworm, use daily for 4 weeks; for jo...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

TOLNAFTATE 1%

Purpose

OTC - PURPOSE SECTION

Anti-fungal

Uses

INDICATIONS & USAGE SECTION

1.For effective treatment of most athlete's foot (tinea pedis), ringworm (tineacorporis)and jock itch (tinea cruris).
2.For effective relief of itching, burning, and cracking skin.
3.For the prevention of most athlete's foot (tinea pedis) with daily use.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

Avoid contact with the eyes.If contact occurs, rinse thoroughly with water.
Use only as directed.

Stop use and ask a doctor if

OTC - STOP USE SECTION

For the treatment of athlete's foot and ringworm:if irritation occurs or if there is no improvement within 4 weeks,discontinue use and consult a doctor.
For the treatment of jock itch:if irritation occurs or if there is no improvement within 2 weeks, discontinue use and consult a doctor.

Do Not Use

OTC - DO NOT USE SECTION

​
On broken, irritated, or severely damaged skin.Do not use on children under 2 years of age unless directed by a doctor.Do not use for diaper rash.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wash he affected area and dry thoroughly. Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor Supervise children in the use of this product.

For athlete's foot: pay special attention to spaces between the toes; wear wellfitting, ventilated shoes, and change shoes and socks at least once daily. For athlete's foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks. If condition persists longer, consult a doctor. This product is not effective on the scalp or nails.

Inactive ingredients

INACTIVE INGREDIENT SECTION

STEARIC ACID, MYRISTIC ACID, AQUA, SUCROSE,LAURIC ACID, COCOYL GLUTAMIC ACID, SODIUM HYDROXIDE, SODIUM CITRATE, LONICERA JAPONIC (HONEYSUCKLE) EXTRACT, PROPYLENE GLYCOL,SODIUM LAURYL SULFATE, COCOS NUCIFERA (COCONUT) OIL, MELALEUCA ALTERNIFOLIA (TEA TREE) OIL,SULFUR SPRING EXTRACT, SORBITOL, GLYCERIN, ARTEMISIA ARGYI EXTRACT

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABELLABEL

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-62083566-620-01

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#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
VXGXO antifungal with tea tree oilTOLNAFTATEGuangdong Aimu Biological Technology Co., Ltd58fd67c5-c985-13a7-e063-6294a90a40fb2026-08-14WarningsExact identifier
ndc (package): 83566-620-01
ndc (product): 83566-620
ndc11 (package): 83566062001
spl id: 58fd67c5-c986-13a7-e063-6294a90a40fb
spl set id: 58fd67c5-c985-13a7-e063-6294a90a40fb

Reported adverse events (FAERS/openFDA)#

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