NDC 42432-101-05 - 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
- 42432-101-05
- 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 |
|---|---|---|---|---|---|---|
| FLUSH Maximum Strength Antifungal formula | UNDECYLENIC ACID | Triple Point Group, LLC | 1d9e56ef-c7c9-4aff-ab9e-b163e566e3d5 | 2023-11-11 | Warnings | K3D86KJ24N |
| CLARUS AC Antifungal Solution | TOLNAFTATE | Clinical Therapeutic Solutions | 28ab9f1b-65cd-4405-a9a3-f3c9b836693d | 2023-11-10 | Warnings | 313423 06KB629TKV |
| Signature Black Bottle Tea Tree Antifungal Foot and Body Wash | TOLNAFTATE | Restoration Rockstar, Llc (dba: Kroning Signature Black Bottle) | 2c966d97-30f5-4942-b64d-742884ce6a2f | 2023-11-10 | Warnings | 06KB629TKV |
| TOLNAFTATE ANTIFUNGAL | TOLNAFTATE | Geri-Care Pharmaceuticals, Corp | f9e60430-eec1-4bc2-9522-eb5aa527d90a | 2023-11-08 | Warnings | 06KB629TKV |
| EmoniNail Antifungal | UNDECYLENIC ACID | GG Healthworks Inc. | 84ace47a-d3ae-4735-87b6-dbbf1c40cf54 | 2023-11-06 | Warnings | K3D86KJ24N |
| CIDACIN Antifungal Treatment | TOLNAFTATE | Pedicis Research LLC | bd53a9e3-65c8-4834-8e23-a2a928b83a66 | 2023-11-05 | Warnings | 313423 06KB629TKV |
| CLARUS Antifungal | TOLNAFTATE | Clinical Therapeutic Solutions | 7e8897ff-67d1-4336-866e-cb76a36edddc | 2023-11-05 | Warnings | 06KB629TKV |
| CLARUS Antifungal | TOLNAFTATE | Clinical Therapeutic Solutions | 308a91d1-3511-4e2d-a62f-a31d77d70e06 | 2023-11-05 | Warnings | 313423 06KB629TKV |
| Human Science Antifungal Foot Care | UNDECYLENIC ACID | HUMAN SCIENCE, LLC | 26b2519b-7d7b-4b33-b5d6-a41fe6f73538 | 2023-11-05 | Warnings | K3D86KJ24N |
| HomeHealth Antifungal | TOLNAFTATE | Home Health | 895cd24c-3f78-4e2e-bf98-8bb6605798da | 2023-11-05 | Warnings | 06KB629TKV |
| CR-371059 Tolnaftate 1% | CR-371059 TOLNAFTATE 1% | A-S Medication Solutions | bb4e4612-850c-4863-954d-7ad0500b9c05 | 2023-11-01 | Warnings | 06KB629TKV |
| Thera plus Antifungal Tolnaftate | TOLNAFTATE | FOURSTAR GROUP USA, INC. | c628dda8-7a6d-5f3a-e053-2995a90a35f8 | 2023-10-26 | Warnings | 06KB629TKV |
| Pollutox | SULPHURICUM ACIDUM, BERBERIS VULGARIS, ARSENICUM ALBUM, BENZINUM, CADMIUM SULPHURATUM, HYDROFLUORICUM ACIDUM, MELATONIN, NITROGENUM OXYGENATUM, NUX VOMICA, PETROLEUM, PLUMBUM METALLICUM, STANNUM METALLICUM, TOLUENE, ACETONE, CARBON DIOXIDE, CHLORINUM, MERCURIUS SOLUBILIS, URANIUM NITRICUM, OZONE | Deseret Biologicals, Inc. | 14a1f0a6-1b22-449c-b4dd-f8feb7215554 | 2023-10-26 | Warnings | 1364PS73AF |
| Mycozyl AL | TOLNAFTATE | PURETEK CORPORATION | 07edd043-4ac4-b2de-e063-6394a90af25d | 2023-10-17 | Warnings, Adverse reactions | 313423 06KB629TKV |
| ANUBISMED | HA HYALURONIC | ANUBIS COSMETICS SL | eac771e2-4c1b-3808-e053-2995a90ac5fc | 2023-09-05 | Warnings | 6DC9Q167V3 ZY81Z83H0X 059QF0KO0R |
| AnubisMed | SPF 50 BROAD SPECTRUM PROTECTION FLUID EMULSION | ANUBIS COSMETICS SL | e99d92c4-8768-9c0a-e053-2a95a90a609e | 2023-09-05 | Warnings | 6DC9Q167V3 059QF0KO0R |
| AnubisMed | AZELAIC ACID, SALICYLIC ACID | ANUBIS COSMETICS SL | ebf3153d-30f5-54e4-e053-2995a90a74b1 | 2023-09-05 | Warnings | 6DC9Q167V3 059QF0KO0R |
| AnubisMed | GLYCOLIC ACID, CITRIC ACID, LACTIC ACID, KOJIC ACID | ANUBIS COSMETICS SL | eca95dde-cb57-2ab6-e053-2995a90af84f | 2023-09-05 | Warnings | 6DC9Q167V3 059QF0KO0R |
| AnubisMed | SODIUM BICARBONATE, ALOE BARBADENSIS LEAF JUICE, IMIDAZOLIDINYL UREA | ANUBIS COSMETICS SL | ebf4b3ab-34e1-185a-e053-2a95a90ace3a | 2023-09-05 | Warnings | ZY81Z83H0X 059QF0KO0R |
| Anubis Barcelona | GLYCERIN, SORBITOL, ALOE BARBADENSIS LEAF JUICE | ANUBIS COSMETICS SL | eb651769-4d98-2b3b-e053-2a95a90a36b0 | 2023-09-01 | Warnings | ZY81Z83H0X 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.