Inlifay ANTIFUNGAL

Manufacturer
Guangzhou Haishi Biological Technology Co., Ltd.
Effective date
2025-10-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:39:19

Label at a glance#

ProductInlifay ANTIFUNGAL
Active ingredientTOLNAFTATE
Label structure11 sections

Indications and uses

Apply to the body and feet during a shower or bath.Gently massage over the entire body, paying specialattention to areas prone to odor or skin irritation.After washing, rinse and dry the skin and feetthoroughly. children must use this product underadult supervision. For best results, use daily for twoweeks.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

TOLNAFTATE 1%

Purpose

OTC - PURPOSE SECTION

USES Helps relieve and prevent the itching, burning, cracking, and scalingassociated with fungal infections-such as athlete's foot, jock itch, andringworm-as well as other skin irritations.

Uses

INDICATIONS & USAGE SECTION

Apply to the body and feet during a shower or bath.Gently massage over the entire body, paying specialattention to areas prone to odor or skin irritation.After washing, rinse and dry the skin and feetthoroughly. children must use this product underadult supervision. For best results, use daily for twoweeks.

Warnings

WARNINGS SECTION

For external use only, Do not use if m You are pregnant or breastfeeding.
You have an allergic reaction to tolnaftate.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if: mlrritation occurs

Do Not Use

OTC - DO NOT USE SECTION

Do not use on children under 2 years of age unless directed by a doctor.

When Using

OTC - WHEN USING SECTION

When using this product m Avoid contact with eyes. lf contact occurs, rinse thoroughw with water

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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

STEARIC ACID 26%
MYRISTIC ACID 12%
AQUA 10%
SUCROSE 10%
LAURIC ACID 8%
COCOYL GLUTAMIC ACID 8%
SODIUM HYDROXIDE 5%
SODIUM CITRATE 4%
LONICERA JAPONICA (HONEYSUCKLE) EXTRACT 3%

PROPYLENE GLYCOL 2%
SODIUM LAURYL SULFATE 2%
COCOS NUCIFERA (COCONUT) OIL 2%
MELALEUCA ALTERNIFOLIA (TEA TREE) OIL 2%
SULFUR SPRING EXTRACT 2%
SORBITOL 1%
GLYCERIN 1%
ARTEMISIA ARGYI EXTRACT 1%

Dosage & administration

DOSAGE & ADMINISTRATION SECTION

Take an appropriate amount of soap, lather by rubbing, apply to the area to be cleaned, gently massage for 1-2 minutes, then rinse thoroughly with water

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label.Label.

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1807715tolnaftate 1 % Medicated Bar SoapPSN1
1807715tolnaftate 0.01 MG/MG Medicated Bar SoapSCD1
1807715tolnaftate 1 % Medicated Bar SoapSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130860013143848GTIN-13: 0860013143848
EAN-13: 0860013143848
GTIN-12: 860013143848
UPC-A: 860013143848
GTIN storage (14 digits): 00860013143848
00_01.jpg

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
60771-0040-1Inlifay ANTIFUNGAL232 g in 1 BOXSOAP2321

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60771-004060771-0040-1

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
Inlifay ANTIFUNGALTOLNAFTATEGuangzhou Haishi Biological Technology Co., Ltd.4141574d-7a5b-c437-e063-6394a90aacb62025-10-16WarningsExact identifier
ndc (package): 60771-0040-1
ndc (product): 60771-0040
ndc11 (package): 60771004001
spl id: 4141574d-7a5c-c437-e063-6394a90aacb6
spl set id: 4141574d-7a5b-c437-e063-6394a90aacb6

Reported adverse events (FAERS/openFDA)#

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