NDC 87161-444-01 - Boka Sensitive
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
- 87161-444
- Requested NDC
- 87161-444-01
- Package NDCs from labels
- 87161-444-01, 87161-444-02, 87161-444-03
- Manufacturer
- Karaka LLC | Northwest Cosmetic Laboratories L.L.C. DBA Elevation Labs, Idaho
- Effective date
- 2025-10-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| WATER - Karaka LLC | Northwest Cosmetic Laboratories L.L.C. DBA Elevation Labs, Idaho | Karaka LLC | Northwest Cosmetic Laboratories L.L.C. DBA Elevation Labs, Idaho | 2025-10-23 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 87161-444-01 | Boka Sensitive | 96 g in 1 TUBE | PASTE, DENTIFRICE | 96 | 2 | |
| 87161-444-02 | Boka Sensitive | 1 in 1 BOX | PASTE, DENTIFRICE | 1 | 2 | |
| 87161-444-03 | Boka Sensitive | 113 g in 1 TUBE | PASTE, DENTIFRICE | 113 | 2 |
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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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.