FUNGAL NAIL LIQUID- tolnaftate liquid

Fungal Nail Liquid by

Drug Labeling and Warnings

Fungal Nail Liquid by is a Otc medication manufactured, distributed, or labeled by Shenzhen Yangan Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

FUNGAL NAIL LIQUID

ACTIVE INGREDIENT

Tolnaftate 1%

PURPOSE

Antifungal

INDICATIONS & USAGE

for relief and treatment of pain,soreness,and inflammation from nail fungus.
Symptoms:
discolored nails
brittle nails
nail splitting
distorted nails

WARNINGS

For external use only

DO NOT USE

Stop Use And See A Doctor IfYou become pregnant or areplanning to get pregnant whileusing the product.You are allergic to this product(such as itching, rash swelling ofthe lips, eyelids, and shortness ofbreath).

WHEN USING

When Using
Stop Use And See A Doctor IfYou become pregnant or areplanning to get pregnant whileusing the product.You are allergic to this product(such as itching, rash swelling ofthe lips, eyelids, and shortness ofbreath).

STOP USE

If skin becomes red and swollen, or if burning, aching and other forms ofirritation occur, cease using and seek medical advice at once.

If you are allergic to this product. Ifsymptoms persist for over 7 days orworsen, consult your physician.Ifyou are pregnant or breast-feeding You become pregnant or areplanning to

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Do not use on children under 2 yearsof age unless directed by a doctorAvoid contact with eyes, ears or mouthIf irritation occurs, discontinue useand consult a doctorIf swallowed, get medical help orconsult a poison control centerimmediately

STORAGE AND HANDLING

Store in a cool and dry place.

INACTIVE INGREDIENT

Water
Acetic Acid
Sophora Flavescens
Lonicerae Japonicae flos
Angelicae
Glycerin
Allantoin
Garlic Extract
Tea Tree Oi

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FUNGAL NAIL LIQUID 
tolnaftate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84023-501
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 mL

Inactive Ingredients
Ingredient Name	Strength
ACETIC ACID (UNII: Q40Q9N063P)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
ANGELICA ACUTILOBA ROOT (UNII: 3W51R3EK30)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALLANTOIN (UNII: 344S277G0Z)
GARLIC (UNII: V1V998DC17)
TEA TREE OIL (UNII: VIF565UC2G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84023-501-01	1 in 1 BOX	03/08/2024
1		15 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	03/08/2024

Labeler - Shenzhen Yangan Technology Co., Ltd. (419283765)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Yangan Technology Co., Ltd.		419283765	manufacture(84023-501)