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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| Q Skin Science | SUNSCREEN | International Cosmeceuticals, Inc | 59e4c3d0-ee4c-2350-e063-6394a90ac9d2 | 2026-08-25 | Warnings | 15FIX9V2JP |
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| TheraBreath | POTASSIUM NITRATE, SODIUM FLUORIDE | Church & Dwight Co., Inc. | 4b812a38-f7cb-51c8-e063-6394a90ab82c | 2026-08-21 | Warnings | M021 8ZYQ1474W7 |
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| COLGATE OPTIC WHITE PRO SERIES EXPRESS WHITE | SODIUM MONOFLUOROPHOSPHATE | Colgate-Palmolive Company | 188dc3ac-64c9-438e-858b-846f725c6ea0 | 2026-08-21 | Warnings | M021 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.