INLIFAY ANTIFUNGAL- tolnaftate soap

Inlifay ANTIFUNGAL by

Drug Labeling and Warnings

Inlifay ANTIFUNGAL by is a Otc medication manufactured, distributed, or labeled by Guangzhou Haishi Biological Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

TOLNAFTATE 1%

Purpose

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

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

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

Stop Use

Stop use and ask a doctor if: mlrritation occurs

Do Not Use

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

When Using

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

Keep Out Of Reach Of Children

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

Inactive ingredients

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

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

INGREDIENTS AND APPEARANCE

INLIFAY ANTIFUNGAL 
tolnaftate soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60771-0040
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SUCROSE (UNII: C151H8M554)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)
SORBITOL (UNII: 506T60A25R)
GLYCERIN (UNII: PDC6A3C0OX)
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)
LAURIC ACID (UNII: 1160N9NU9U)
COCOYL GLUTAMIC ACID (UNII: 05F3H883OB)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SULFUR (UNII: 70FD1KFU70)
AQUA (UNII: 059QF0KO0R)
STEARIC ACID (UNII: 4ELV7Z65AP)
ARTEMISIA ARGYI LEAF (UNII: 2JYC99Q0WZ)
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
MYRISTIC ACID (UNII: 0I3V7S25AW)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60771-0040-1	232 g in 1 BOX; Type 0: Not a Combination Product	10/16/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	10/16/2025

Labeler - Guangzhou Haishi Biological Technology Co., Ltd. (421262738)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Haishi Biological Technology Co., Ltd.		421262738	manufacture(60771-0040)