PHYTOZINE RINGWORM TREATMENT
- Product NDC
- 71229-101
- 11-digit product format
- 712290101
- Labeler code
- 71229
- Product ID
- 71229-101_334f4f69-fe0c-c703-e063-6394a90adecf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TOLNAFTATE
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- The Sisquoc Healthcare Corporation
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-03-25
- Substance
- TOLNAFTATE
- Active strength
- 1 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded product | product | 302b2466d912… | e7b80fea0513… | |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 71229-101-11 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 71229-101-11 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 71229-101-11 | 0efc9e666f02… | f202fb6c5f17… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PHYTOZINE RINGWORM TREATMENT
- Brand name suffix
- MAXIMUM STRENGTH
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| TOLNAFTATE | 1 g/100g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 06KB629TKV | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 199126 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 5dff6ee7-f7a9-4841-8357-6b0801d253f1 | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
| Effective | Related label |
|---|---|
| 2025-02-25 | Sisquoc HC (as PLD) - PHYTOZINE RINGWORM TREATMENT (71229-101) |
| 2025-01-30 | Sisquoc HC (as PLD) - PHYTOZINE RINGWORM TREATMENT (71229-101) |
| 2022-03-18 | Sisquoc HC (as PLD) - PHYTOZINE RINGWORM TREATMENT (71229-101) |
| 2022-01-28 | Sisquoc HC (as PLD) - PHYTOZINE RINGWORM TREATMENT (71229-101) |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71229-101-11 | PHYTOZINE RINGWORM TREATMENTMAXIMUM STRENGTH | 28 g in 1 TUBE | OINTMENT | 28 | 6 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| MICONAZOLE Nitrate 2% Cream ANTIFUNGAL | MICONAZOLE NITRATE | ASTONEA LABS PRIVATE LIMITED | e66191a6-0c3c-7319-e053-2a95a90aae84 | 2024-06-25 | Warnings | M005 |
| clotrimazole | CLOTRIMAZOLE | A-S Medication Solutions | b63a3fe5-5684-41bc-ad6c-69c54e5b942d | 2024-06-20 | Warnings | M005 |
| THERA Antifungal Body | MICONAZOLE NITRATE | McKesson Medical-Surgical Inc. | 31096041-28c9-4b16-bbd1-dbadefd37505 | 2024-06-14 | Warnings | M005 |
| Antifungal Body | MICONAZOLE NITRATE | McKesson | 4fb9aece-0baa-475e-e054-00144ff8d46c | 2024-06-13 | Warnings | M005 |
| Secura Protective | ZINC OXIDE | Smith & Nephew Medical Ltd | b077aa64-49a3-42ee-abb3-88f833635b93 | 2024-06-12 | Warnings | M005 |
| clotrimazole | CLOTRIMAZOLE | NuCare Pharmaceuticals,Inc. | 627375fb-2f20-16bc-e053-2a91aa0a1542 | 2024-06-06 | Warnings | M005 |
| Clotrimazole | CLOTRIMAZOLE | Cardinal Health 110 dba LEADER | 199df107-3384-6e03-e063-6294a90afc38 | 2024-05-29 | Warnings | M005 |
| Femmesil | CLOTRIMAZOLE | Aidance Skincare & Topical Solutions, LLC | efddad82-9dc7-4cd9-b33c-7e85f30d992e | 2024-05-24 | Warnings | M005 |
| Anti-Fungal | MICONAZOLE NITRATE | Universal Distribution Center LLC | 8f316b0d-d308-4ae6-82c4-39bb0d1d474e | 2024-05-21 | Warnings | M005 |
| CANESPIES | TOLNAFTATE | OPMX LLC | e2f9eedc-3c43-416b-85b5-ba07fb5fb4db | 2024-05-17 | Warnings | M005 |
| Up and Up Antifungal | TOLNAFTATE 1% | Target Corporation | 8f54c8c7-6771-49c3-b429-53aa6df54dc5 | 2024-05-08 | Warnings | M005 |
| Up and Up Athletes Foot | CLOTRIMAZOLE 1% | Target Corporation | 52b61859-11ae-4990-aa0c-9dc1dd00adf4 | 2024-05-08 | Warnings | M005 |
| ADI Medical PVP-I Pouch, Foil | POVIDONE-IODINE | Asia Dynamics Inc., d/b/a ADI Medical | 0e8baf24-0c67-5511-e063-6394a90acaa1 | 2024-05-02 | Warnings | M005 |
| Caseys Antimicrobial Hand Sanitizer | ETHYL ALCOHOL | Navajo Manufacturing Company Inc. | 78863024-390c-4ff9-8ed6-02af07902a30 | 2024-04-29 | Warnings | M005 |
| MQUPIN Liquid Fungal Nail Treatment | LIQUID FUNGAL NAIL TREATMENT | Zhengzhou Miaoqi Medical Technology Co., Ltd. | 14782f8c-3b29-1d88-e063-6294a90ac3e4 | 2024-03-25 | Warnings | M005 |
| ETADERM Advanced Antifungal Support | UNDECYLENIC ACID | NUEPHASE LLC | adb12a1c-ece9-4a59-a62c-89d212c57e6f | 2024-03-13 | Warnings | M005 |
| Dermachange Jock | MICONAZOLE NITRATE | Private label Beauty and Wellness | 12eef049-76c9-1450-e063-6394a90a00ea | 2024-03-05 | Warnings | M005 |
| Clotrimazole Antifungal | CLOTRIMAZOLE | Trifecta Pharmaceuticals USA, LLC. | 11bf50db-552e-0a39-e063-6394a90af60d | 2024-02-19 | Warnings | M005 |
| TOLNAFTATE ANTIFUNGAL | TOLNAFTATE | Bryant Ranch Prepack | fbbd159c-217e-46d3-963c-ba0bd1e9bbe8 | 2024-01-29 | Warnings | M005 |
| Target Jock Itch | CLOTRIMAZOLE 1% | Target Corporation | f44d4c44-99d1-413f-b9c3-8330bdd21abb | 2024-01-17 | Warnings | M005 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 199126 | tolnaftate 1 % Topical Ointment | PSN | 5dff6ee7-f7a9-4841-8357-6b0801d253f1 | 6 |
| 199126 | tolnaftate 0.01 MG/MG Topical Ointment | SCD | 5dff6ee7-f7a9-4841-8357-6b0801d253f1 | 6 |
| 199126 | tolnaftate 1 % Topical Ointment | SY | 5dff6ee7-f7a9-4841-8357-6b0801d253f1 | 6 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 71229-101-11 | 71229010111 | 28 g in 1 TUBE (71229-101-11) | 28 g | 2019-03-25 | 0000-00-00 | No | No | Current |