FDA.reportPublic FDA data

APUREE Nailtific Maximum Strength Antifungal Patches PRO

Manufacturer
Guangzhou Meixi Biotechnology Co., Ltd | Guangzhou Meixi Biotechnology Co., Ltd.
Effective date
2026-05-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:56:53

Label at a glance#

ProductAPUREE Nailtific Maximum Strength Antifungal Patches PRO
Active ingredientTOLNAFTATE
Label structure7 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

keep out of children

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

INDICATIONS & USAGE SECTION

Antifungal

DOSAGE & ADMINISTRATION SECTION

8 Hour

INACTIVE INGREDIENT SECTION

Aqua,Urea,Lactic Acid,Terpinen-4-ol,Glycerin,Polyacrylamide,
Seaweed Extract,Panthenol,Tocopheryl Acetate,Bisabolol,
Allantoin,Mentha Arvensis Leaf Oil,Menthol & Essential Oil Complex

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

33

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2677690tolnaftate 1 % Medicated PatchPSN1
2677690tolnaftate 0.01 MG/MG Medicated PatchSCD1
2677690tolnaftate 1 % Medicated PatchSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codewww.apuree.com/0.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84167-416-01APUREE Nailtific Maximum Strength Antifungal Patches PRO2 in 1 BOXPATCH21
84167-416-01APUREE Nailtific Maximum Strength Antifungal Patches PRO32 in 1 PATCHPATCH321

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84167-41684167-416-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-BISABOLOL, (+/-)-36HQN158VCIACT
LACTIC ACID, DL-3B8D35Y7S4IACT
DEXPANTHENOL1O6C93RI7ZIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
MENTHA PIPERITA (PEPPERMINT) OILAV092KU4JHIACT
UREA8W8T17847WIACT
HYPOCHLOROUS ACID712K4CDC10IACT
ALLANTOIN344S277G0ZIACT
TOLNAFTATE06KB629TKVACTIB
GLYCERINPDC6A3C0OXIACT
MENTHA ARVENSIS LEAF OIL1AEY1M553NIACT
AQUA059QF0KO0RIACT
4-TERPINEOLL65MV77ZG6IACT
POLYACRYLAMIDE (1500 MW)5D6TC4BRWVIACT

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
APUREE Nailtific Maximum Strength Antifungal Patches PROAPUREE NAILTIFIC MAXIMUM STRENGTH ANTIFUNGAL PATCHES PROGuangzhou Meixi Biotechnology Co., Ltd5189ebc5-8ee5-1b2c-e063-6294a90af5c82026-05-11WarningsExact identifier
ndc (package): 84167-416-01
ndc (product): 84167-416
ndc11 (package): 84167041601
spl id: 5189ebc5-8ee6-1b2c-e063-6294a90af5c8
spl set id: 5189ebc5-8ee5-1b2c-e063-6294a90af5c8

Reported adverse events (FAERS/openFDA)#

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