APUREE NAILTIFIC EXTRA-MAX STRENGTH NIGHTTIME ANTIFUNGAL liquid

APUREE Nailtific Extra-Max Strength Nighttime Antifungal by

Drug Labeling and Warnings

APUREE Nailtific Extra-Max Strength Nighttime Antifungal by is a Otc medication manufactured, distributed, or labeled by Guangzhou Meixi Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Tolnaftate

DOSAGE & ADMINISTRATION

Apply directly to the affected area

KEEP OUT OF REACH OF CHILDREN

keep out of reach of child

INDICATIONS & USAGE

Antibacterial and anti-itch

WARNINGS

PURPOSE

15-Day & 15-Night Supply

INACTIVE INGREDIENT

Simmondsia Chinensis Seed Oil,Caprylic/Capric Triglyceride,Pentaerythrityl Tetra-Di-T-Butyl Hydroxyhydrocinnamate,Melaleuca Alternifolia Leaf Oil,Cinnamomum Cassia Oil,Origanum Vulgare Oil,Calophyllum Inophyllum Seed Oil,Eugenia Caryophyllus Bud Oil,Eucalyptus Globulus Leaf Oil,Lavandula Angustifolia Oil

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

APUREE NAILTIFIC EXTRA-MAX STRENGTH NIGHTTIME ANTIFUNGAL 
apuree nailtific extra-max strength nighttime antifungal liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84167-479
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
ORIGANUM VULGARE LEAF OIL (UNII: 7D0CGR40U1)
CINNAMOMUM CASSIA OIL (UNII: A4WO0626T5)
EUGENIA CARYOPHYLLUS (CLOVE) BUD OIL (UNII: 578389D6D0)
SIMMONDSIA CHINENSIS SEED WAX (UNII: 47X6Y9FJJ2)
PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE (UNII: 255PIF62MS)
LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL (UNII: ZBP1YXW0H8)
MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
CALOPHYLLUM INOPHYLLUM SEED OIL (UNII: JT3LVK84A1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84167-479-02	1 in 1 BOX	03/30/2026
1		30 in 1 VIAL, SINGLE-USE; 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	03/30/2026

Labeler - Guangzhou Meixi Biotechnology Co., Ltd. (625724571)

Registrant - Guangzhou Meixi Biotechnology Co., Ltd. (625724571)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Meixi Biotechnology Co., Ltd.		625724571	manufacture(84167-479) , label(84167-479)