INLIFAY ANTIFUNGAL- tolnaftate soap

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredients

Tolnaftate 1%

Purpose

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.

Warnings

For external use only.

Stop Use

The condition persists for more than 2 weeks or worsens.

you experience side effects such as skin redness or irritation at the application site.

Do Not Use

Do not use on broken, irritated, or severely damaged skin.

Do not use for diaper rash. children under 2 years of age unless directed by a doctor.

When Using

Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Keep Out Of Reach Of Children

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

Dosage & administration

Apply to the body and feet during a shower or bath.For best results, use daily for twoweeks.

Inactive ingredients

Aqua (Water), Melaleuca Alternifoha (Tea Tree) LeafOil, Sorbitol , ElaeisGuineensis (Palm) Oil , Cocos Nucifera (Coconut) Oil , Olea Europaea (Olive) Fruit Oil, Propylene Glycol ,Glycerin, Stearic Acid, Lauric Acid ,Myristic Acid, Sodium Myristate , Sodium Glutamate , SodiumHydroxide, Sodium Dodecylbenzene Sulfonate, Sulfur Thermal Water, Hamamelis Virginiana (Witch Hazel)Extract,Ceramide

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

INLIFAY ANTIFUNGAL 
tolnaftate soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83566-609
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
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)
CERAMIDE 3 (UNII: 4370DF050B)
AQUA (UNII: 059QF0KO0R)
ELAEIS GUINEENSIS (PALM) OIL (UNII: 5QUO05548Z)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM GLUTAMATE (UNII: W81N5U6R6U)
SORBITOL (UNII: 506T60A25R)
OLEA EUROPAEA (OLIVE) FRUIT OIL (UNII: 6UYK2W1W1E)
GLYCERIN (UNII: PDC6A3C0OX)
STEARIC ACID (UNII: 4ELV7Z65AP)
LAURIC ACID (UNII: 1160N9NU9U)
MYRISTIC ACID (UNII: 0I3V7S25AW)
SODIUM MYRISTATE (UNII: 06BLC4V0IV)
HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER (UNII: 8FP93ED6H2)
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)
SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83566-609-01	232 g in 1 BOX; Type 0: Not a Combination Product	05/09/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	05/09/2026

Labeler - Guangdong Aimu Biological Technology Co., Ltd (712647107)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Aimu Biological Technology Co., Ltd		712647107	manufacture(83566-609)