NDC 57577-077-01 - DCL Zoma
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
- 57577-077
- Requested NDC
- 57577-077-01
- Package NDCs from labels
- 57577-077-01, 57577-077-02
- Manufacturer
- Milbar Laboratories | Milbar Labs, Inc
- Effective date
- 2024-04-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| DCL Zoma - Milbar Laboratories | Milbar Labs, Inc | Milbar Laboratories | Milbar Labs, Inc | 2024-04-10 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 57577-077-01 | DCL Zoma | 236 mL in 1 BOTTLE, DISPENSING | LOTION/SHAMPOO | 236 | 1 | |
| 57577-077-02 | DCL Zoma | 1 in 1 CARTON | LOTION/SHAMPOO | 1 | 1 |
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.
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| Tucks Triple Relief Hemorrhoidal | WHITE PETROLATUM, GLYCERIN, PRAMOXINE HYDROCHLORIDE, AND PHENYLEPHRINE HYDROCHLORIDE | Blistex Inc. | bf892e90-2d9b-4fa0-8ee4-8a2736be6c30 | 2024-12-24 | Warnings | PDC6A3C0OX |
| TREE ANTIGEN | POPULUS TRISTIS POLLEN, JUGLANS NIGRA POLLEN, ACER NEGUNDO POLLEN, ALNUS RUBRA POLLEN, JUNIPERUS VIRGINIANA POLLEN, ULMUS RUBRA POLLEN, ACER PSEUDOPLANUS POLLEN, FRAXINUS AMERICANA POLLEN, CARYA TOMENTOSA POLLEN, ONION, ARSENIC TRIOXIDE, ATROPA BELLADONNA, ACTIVATED CHARCOAL, EUPHRASIA OFFICINALIS, LYCOPODIUM CLAVITUM SPORE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, PULSITILLA VULGARIS WHOLE | Natural Creations, Inc | 8040ab36-90eb-4076-a478-9b82ccfa4ec9 | 2024-12-23 | Warnings | 451W47IQ8X |
| Sterile Hypertonic Saline Solution 7 Sodium Chloride | SODIUM CHLORIDE | JOONEM LLC | e7110525-9f9b-5b68-e053-2995a90ac034 | 2024-12-23 | Warnings | 451W47IQ8X |
| Base Laboratories Saline | SODIUM CHLORIDE | Joonem LLC | 49309411-9af4-4f19-a3bf-dbeabc106827 | 2024-12-23 | Warnings | 451W47IQ8X |
| Base Laboratories Saline | SODIUM CHLORIDE | Joonem LLC | ba0868f6-d3de-40e2-bcb3-144fa53062c7 | 2024-12-23 | Warnings | 451W47IQ8X |
| Base Laboratories Saline | SODIUM CHLORIDE | Joonem LLC | 9d83f477-ebbc-4248-8445-769178181d4f | 2024-12-23 | Warnings | 451W47IQ8X |
| Pedia-Lax | GLYCERIN | C.B. Fleet Company, Inc. | 4e15f6ca-a40c-485f-be3f-07c2ed7cb498 | 2024-12-23 | Warnings | PDC6A3C0OX |
| OASIS Tears Preservative-Free Lubricant Eye | GLYCERIN | OASIS Medical, Inc. | d9d71b1d-82a6-42e7-9ef2-2d041daef936 | 2024-12-23 | Warnings | PDC6A3C0OX |
| Dermaharmony Seborrheic Dermatitis | PYRITHIONE ZINC | D3 Development, Inc. | 8d81521d-9e6f-1acf-e053-2995a90a9242 | 2024-12-20 | Warnings | R953O2RHZ5 |
| Dermaharmony Bar Peppermint | PYRITHIONE ZINC | D3 Development, Inc. | a19b74b0-88c6-6897-e053-2a95a90a7309 | 2024-12-20 | Warnings | R953O2RHZ5 |
| Dermaharmony Face and Body | PYRITHIONE ZINC | D3 Development, Inc. | bd72b53c-b22c-40d0-e053-2995a90af9c1 | 2024-12-20 | Warnings | R953O2RHZ5 |
| Zinc Therapy | PYRITHIONE ZINC | D3 Development, Inc. | 637851c6-ff4a-8bbc-e053-2991aa0a963c | 2024-12-20 | Warnings | R953O2RHZ5 |
| Dermaharmony Zinc Therapy | PYRITHIONE ZINC | D3 Development, Inc. | cb442483-b735-01a0-e053-2995a90aaff5 | 2024-12-20 | Warnings | R953O2RHZ5 |
| Dermaharmony Pyrithione Zinc with Shea Butter | PYRITHIONE ZINC | D3 Development, Inc. | dc7ba02c-bdbd-5136-e053-2995a90ac545 | 2024-12-20 | Warnings | R953O2RHZ5 |
| Dermaharmony Tea Tree Bar | PYRITHIONE ZINC | D3 Development, Inc. | e9d5eb14-1840-ae21-e053-2a95a90aa321 | 2024-12-20 | Warnings | R953O2RHZ5 |
| Dermaharmony Unscented Bar | PYRITHIONE ZINC | D3 Development, Inc. | e9d66c9c-5fb1-0a90-e053-2a95a90ab7a4 | 2024-12-20 | Warnings | R953O2RHZ5 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.