NDC 61596-101-01 - MIPaste One Kids Bubble Gum
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
- 61596-101
- Requested NDC
- 61596-101-01
- Package NDCs from labels
- 61596-101-01, 61596-101-02, 61596-101-10
- Manufacturer
- GC America Inc.
- Effective date
- 2025-12-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| MIPaste One Kids Bubble Gum | GC America Inc. | 2025-12-19 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61596-101-01 | MIPaste One Kids Bubble Gum | 46 g in 1 TUBE | PASTE, DENTIFRICE | 46 | 3 | |
| 61596-101-02 | MIPaste One Kids Bubble Gum | 1 in 1 BOX, UNIT-DOSE | PASTE, DENTIFRICE | 1 | 3 | |
| 61596-101-10 | MIPaste One Kids Bubble Gum | 10 in 1 BOX | PASTE, DENTIFRICE | 10 | 3 |
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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| ACT Restoring Anticavity Fluoride Cool Mint | SODIUM FLUORIDE | Chattem, Inc. | 3409a749-4a1a-4950-8c21-364d1b977af7 | 2025-07-22 | Warnings | M021 8ZYQ1474W7 |
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| Act Total Care Anticavity Fluoride Fresh Mint | SODIUM FLUORIDE | Chattem, Inc. | dc209500-2bf4-42fb-b3a1-d0fb8d63dbd8 | 2025-07-22 | Warnings | M021 8ZYQ1474W7 |
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| PCXX PEPPERMINT APF F | SODIUM FLUORIDE | Ross Healthcare Inc. | 5e86783c-414a-5f46-e053-2991aa0abb3b | 2025-07-21 | 8ZYQ1474W7 | |
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| DENTAL-CHORD | ACETICUM ACIDUM, AMMONIUM MURIATICUM, ARGENTUM METALLICUM, AURUM METALLICUM, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CARBOLICUM ACIDUM, CITRUS LIMONUM, CUPRUM METALLICUM, FERRUM METALLICUM, GLYCYRRHIZA GLABRA, LAPPA MAJOR, MEDULLA OSSIS SUIS, MERCURIUS SOLUBILIS, MYRRHA, NATRUM FLUORATUM, PALLADIUM METALLICUM, PHOSPHORICUM ACIDUM, PHYTOLACCA DECANDRA, SELENIUM METALLICUM, SILICEA, STANNUM METALLICUM, STAPHYSAGRIA, STILLINGIA SYLVATICA, TRIFOLIUM PRATENSE, X-RAY, ZINCUM OXYDATUM | Energetix Corporation | 6c9ba926-7c35-49fd-94d8-988ca0bb772c | 2025-07-15 | Warnings | 8ZYQ1474W7 ETJ7Z6XBU4 E4GA8884NN |
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| Amarte ULTRA VEIL Daily | SUNSCREEN | Amarte USA LLC | 39e9ca98-d0e8-6b8f-e063-6394a90aa366 | 2025-07-15 | Warnings | 15FIX9V2JP |
| Amarte ULTRA VEIL BB Fair | SUNSCREEN | Amarte USA LLC | 39e87950-4103-c2eb-e063-6394a90a0552 | 2025-07-15 | Warnings | 15FIX9V2JP |
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| Flotrex | MULTIVITAMINS, SODIUM FLUORIDE 0.5 MG | PureTek Corporation | 2e0e51f3-ee2c-540d-e063-6294a90a9275 | 2025-07-14 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Flotrex | MULTIVITAMINS, SODIUM FLUORIDE 0.25 MG | PureTek Corporation | 30186998-2121-3ef2-e063-6394a90a513e | 2025-07-14 | Warnings, Adverse reactions | 8ZYQ1474W7 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.