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 |
|---|---|---|---|---|---|---|
| Tolnafate | TOLNAFTATE ATHLETES FOOT POWDER SPRAY TALC FREE | VALU MERCHANDISERS, CO | 9ac97d4a-169b-49ff-aa34-ccb5b43726a1 | 2025-11-24 | Warnings | 06KB629TKV |
| Tolnafate | FOOT ODOR CONTROL POWDER SPRAY | VALU MERCHANDISERS, CO | 51b69b0f-d63f-4fe0-87e6-722f95568761 | 2025-11-24 | Warnings | 06KB629TKV |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | beda35c3-9a8b-47ad-e053-2995a90a7b1b | 2025-11-24 | Warnings | 059QF0KO0R |
| Easy Care First Aid Eyewash | WATER | Tender Corporation | a070aac8-e6d2-ef10-e053-2a95a90aa5b1 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | e07a064b-f680-405c-bbcd-24fac430951e | 2025-11-24 | Warnings | 059QF0KO0R |
| ULINE Eyewash | EYEWASH | Niagara Pharmaceuticals Inc. | 2d7f22d2-320b-6af1-e063-6294a90addc6 | 2025-11-24 | Warnings | 059QF0KO0R |
| Pur-Wash | EYEWASH | Niagara Pharmaceuticals, Inc. | 0d43b1c1-2699-37f1-e054-00144ff88e88 | 2025-11-24 | Warnings | 059QF0KO0R |
| Eyewash Station Additive Concentrate | CHLORHEXIDINE GLUCONATE AND PROPYLENE GLYCOL | Niagara Pharmaceuticals Inc. | 362a6b6d-862d-4322-87a8-5b3a07fbe174 | 2025-11-24 | Warnings | 6DC9Q167V3 |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 777e1559-786f-8d54-e053-2991aa0aa98d | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 7289103a-5cbf-42f4-8848-e827149a43ca | 2025-11-24 | Warnings | 059QF0KO0R |
| Odor-Eaters Athletes Foot | TOLNAFTATE | Blistex Inc. | 20d795d1-2345-4d4f-8439-07ad11ff8f65 | 2025-11-21 | Warnings | 06KB629TKV |
| Multi-Purrose Nail | MULTI-PURROSE NAIL | Jiangxi Zhongteng Pharmaceutical Co., Ltd | 4401e739-b58b-2336-e063-6394a90a8c70 | 2025-11-20 | Warnings | 06KB629TKV |
| Eyewash Additive Concentrate | WATER AND PROPYLENE GLYCOL | Haws Corporation | dd168403-398c-41ff-b1df-d93e4ff39de3 | 2025-11-20 | Warnings | 6DC9Q167V3 059QF0KO0R |
| Derman Antifungal | ZINC UNDECYLENATE | Compania Internacional de Comercio, S.A.P.I de C.V. | 0129d801-90f6-49fd-857f-27d6ba9fc66c | 2025-11-19 | Warnings | K3D86KJ24N |
| Sterile Water | WATER | Fresenius Kabi USA, LLC | fd823bef-c14c-4708-a18a-8aaa8470412f | 2025-11-18 | Warnings, Adverse reactions | 059QF0KO0R |
| Mint Blast Foot and Shoe Antifungal | UNDECYLENIC ACID 10% | SANSAR, LLC | f7fcac19-7b72-4b7a-a28e-669a0eebec9c | 2025-11-15 | Warnings | K3D86KJ24N |
| Lavender Foot and Shoe Antifungal | UNDECYLENIC ACID 10% | SANSAR, LLC | 9db58924-a84d-4763-badb-b3aeb46e1ea6 | 2025-11-15 | Warnings | K3D86KJ24N |
| Citrus Detox Foot and Shoe Antifungal | UNDECYLENIC ACID 10% | SANSAR, LLC | 6585c9f5-a6cb-4534-9a61-ecbb6dcb7bdc | 2025-11-15 | Warnings | K3D86KJ24N |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 3765c251-eb14-d60f-e063-6294a90a6a4d | 2025-11-12 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 37f244fd-c02f-e66a-e063-6394a90aed81 | 2025-11-12 | Warnings | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.