NDC 42432-101-11 - Kiss Fungi-Gone Anti-fungal Treatment
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 42432-101
- Requested NDC
- 42432-101-11
- Package NDCs from labels
- 42432-101-03, 42432-101-04, 42432-101-11, 42432-101-51, 42432-101-05, 42432-101-06
- Manufacturer
- Kiss Products, Inc.
- Effective date
- 2015-02-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Kiss Fungi-Gone Antifungal Treatment - Drug Facts | Kiss Products, Inc. | 2015-02-25 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 42432-101-04 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-0a35-f424-e053-dadaa90a57ce | Kiss Fungi-Gone Antifungal Treatment - Drug Facts |
| 42432-101-06 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-0a35-f424-e053-dadaa90a57ce | Kiss Fungi-Gone Antifungal Treatment - Drug Facts |
| 42432-101-51 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-0a35-f424-e053-dadaa90a57ce | Kiss Fungi-Gone Antifungal Treatment - Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 42432-101-03 | Kiss Fungi-GoneAnti-fungal Treatment | 15 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 15 | 10 | |
| 42432-101-04 | Kiss Fungi-GoneAnti-fungal Treatment | 1 in 1 BOX | LIQUID | 1 | 10 | |
| 42432-101-05 | Kiss Fungi-GoneAnti-fungal Treatment | 30 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 30 | 10 | |
| 42432-101-06 | Kiss Fungi-GoneAnti-fungal Treatment | 1 in 1 BOX | LIQUID | 1 | 10 | |
| 42432-101-11 | Kiss Fungi-GoneAnti-fungal Treatment | 15 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 15 | 10 | |
| 42432-101-51 | Kiss Fungi-GoneAnti-fungal Treatment | 1 in 1 BOX | LIQUID | 1 | 10 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| Antifungal Liquid | TOLNAFTATE | Target Corporation | 3c6dd772-0d26-b659-e063-6294a90a5bf8 | 2026-09-24 | Warnings | 313423 06KB629TKV |
| Defense Antifungal Medicated Bar | TOLNAFTATE | Defense Soap LLC | 812d78ea-a14a-e3a2-e053-2a91aa0a6ff5 | 2026-09-09 | Warnings | 06KB629TKV |
| Pollutox | ACETONE, ARSENICUM ALBUM, BENZINUM, BERBERIS VULGARIS, CADMIUM SULPHURATUM, CARBON DIOXIDE, CARBONEUM SULPHURATUM, CHLORINUM, HYDROFLUORICUM ACIDUM, MELATONIN, MERCURIUS SOLUBILIS, NITROGENUM OXYGENATUM, NUX VOMICA, OZONE, PETROLEUM, PLUMBUM METALLICUM, STANNUM METALLICUM, SULPHURICUM ACIDUM, TOLUENE, URANIUM NITRICUM | Deseret Biologicals, Inc. | 741fdddf-75af-45a2-9875-ee3b08b0decf | 2026-09-08 | Warnings | 1364PS73AF |
| Noicaky FUNGAL NAIL Patches | TOLNAFTATE 1% FUNGAL NAIL PATCHES | Wenzhou Yuyuan Pharmaceutical Co., Ltd. | 5adcc5f7-2d47-2ad7-e063-6294a90a4848 | 2026-09-06 | Warnings | 06KB629TKV |
| LIFE66II ANTIFUNGAL NAIL | UNDECYLENIC ACID 25% ANTIFUNGAL NAIL | Wenzhou Yuyuan Pharmaceutical Co., Ltd. | 5ab83796-0780-3b58-e063-6394a90a2e4e | 2026-09-05 | Warnings | K3D86KJ24N |
| FGPER Topical Antifungal Pen | UNDECYLENIC ACID | Guangzhou ChuanMa International Trading Co.,Ltd. | 5abdcbff-6ab1-2f0a-e063-6294a90a57ef | 2026-09-05 | Warnings | K3D86KJ24N |
| ANTIFUNGAL BODY WASH | TOLNAFTATE | Guangzhou ChuanMa International Trading Co.,Ltd. | 5a695043-f776-df5a-e063-6394a90ac274 | 2026-09-01 | Warnings | 06KB629TKV |
| DrAny NAIL FUNGUS TREATMENT | UNDECYLENIC ACID, TOLNAFTATE | Hong Kong Juxin Negosyo Kag Komersyo Co., Limited | 59ef412b-fc7b-0a84-e063-6394a90abf25 | 2026-08-26 | Warnings | 06KB629TKV K3D86KJ24N |
| KUGIG ALOE FOAMING INTIMATE WASH | INTIMATE CLEANSING FOAM | Hong Kong KangXing Centennial Management Limited | 59f4d398-1186-a168-e063-6294a90ab44b | 2026-08-26 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | REMEDYREPACK INC. | 5dd5d148-6e23-41de-bff5-551b2aea9598 | 2026-08-24 | Warnings, Adverse reactions | 059QF0KO0R |
| JELVOXA ANTIFUNGAL | UNDECYLENIC ACID | Wuhan Ruihengjie Technology Co., Ltd. | 59a2f16e-ef72-f1cb-e063-6394a90abb28 | 2026-08-22 | Warnings | K3D86KJ24N |
| ANTIFUNGAL NAIL | UNDECYLENIC ACID | Guangzhou Huanmei Cosmetics Co., Ltd. | 598b9712-001c-4148-e063-6394a90a97b1 | 2026-08-21 | Warnings | 06KB629TKV K3D86KJ24N |
| BlissCare tea tree oil antifungal | TOLNAFTATE | Guangdong Aimu Biological Technology Co., Ltd | 58f9ff8c-d75a-ad1d-e063-6294a90af3dc | 2026-08-21 | Warnings | 06KB629TKV |
| GPPEE TOENAIL FUNGUS TREATMENT | UNDECYLENIC ACID 25% | Guangzhou Huixue Biotechnology Co., Ltd. | 598d05bc-459d-71cf-e063-6394a90a1932 | 2026-08-21 | Warnings | K3D86KJ24N |
| Rohto Optic Glow | NAPHAZOLINE HYDROCHLORIDE, POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | df9c5f7c-96e6-4b2b-b8cb-21a6a3342dff | 2026-08-20 | Warnings | 6DC9Q167V3 |
| Rohto Max Strength | NAPHAZOLINE HYDROCHLORIDE, POLYSORBATE 80 | The Mentholatum Company | e4b49550-1ca3-4bd7-854d-409b53fa5e26 | 2026-08-20 | Warnings | 6OZP39ZG8H |
| Rohto Preservative Free Dry Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | f4b1974c-2412-45f6-b79d-88b8a0bcb608 | 2026-08-18 | Warnings | 6DC9Q167V3 |
| Rohto Dry-Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | 8ea5c6c9-48f4-406a-a2cb-9280c546d87d | 2026-08-18 | Warnings | 6DC9Q167V3 |
| FUNGAL NAIL PATCHES | TOLNAFTATE | Yunqi Cosmetics (Shenzhen) Co., Ltd | 5939c492-6481-ddae-e063-6294a90a40bb | 2026-08-17 | Warnings | 06KB629TKV |
| VXGXO antifungal with tea tree oil | TOLNAFTATE | Guangdong Aimu Biological Technology Co., Ltd | 58fd67c5-c985-13a7-e063-6294a90a40fb | 2026-08-14 | Warnings | 06KB629TKV |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.