Cureforte Anti Fungal Foot Care
- Manufacturer
- STEEL CITY HEALTH PRIVATE LIMITED | Guangdong Aimu Biological Technology Co,Ltd | Guangdong Aimu Biological Technology Co., Ltd
- Effective date
- 2025-08-11
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 01:10:52
Label at a glance#
ProductCureforte Anti Fungal Foot Care
Active ingredientTOLNAFTATE
Label structure7 sections
Label contents#
Full prescribing information#
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
WARNINGS SECTION
DOSAGE & ADMINISTRATION SECTION
INDICATIONS & USAGE SECTION
INACTIVE INGREDIENT SECTION
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 85884-252-02 | Cureforte Anti Fungal Foot Care | 1 in 1 BOX | LIQUID | 1 | 2 | |
| 85884-252-02 | Cureforte Anti Fungal Foot Care | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 2 |
Products#
Every source-derived product name is available through these pages.
- Cureforte Anti Fungal Foot Care
- Anti Fungal Foot Care Drops
- MELALEUCA CAJUPUTI LEAF OIL
- EUCALYPTUS GLOBULUS LEAF OIL
- ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL
- JOJOBA OIL
- CINNAMOMUM CAMPHORA (CAMPHOR) BARK OIL
- TOLNAFTATE
- OREGANO LEAF OIL
- MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 85884-252 | 85884-252-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Cureforte Anti Fungal Foot Care | ANTI FUNGAL FOOT CARE DROPS | STEEL CITY HEALTH PRIVATE LIMITED | 39f762a6-9d0c-8ded-e063-6394a90a3659 | 2025-08-11 | Warnings | 85884-252-02 85884-252 85884025202 3c169b78-0e18-bd86-e063-6394a90a1efe 39f762a6-9d0c-8ded-e063-6394a90a3659 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.


