NDC 70970-100-01 - OHTrust Nano Ion Water
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
- 70970-100
- Requested NDC
- 70970-100-01
- Package NDCs from labels
- 70970-100-01, 70970-100-02
- Manufacturer
- Nanoplus Limited (Cayman) Taiwan Branch
- Effective date
- 2016-09-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| OHTrust Nano Ion Water - Nanoplus Limited (Cayman) Taiwan Branch | Nanoplus Limited (Cayman) Taiwan Branch | 2016-09-26 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70970-100-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-2757-f424-e053-dadaa90a57ce | OHTrust Nano Ion Water |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70970-100-01 | OHTrust Nano Ion Water | 100 mL in 1 BOTTLE, SPRAY | LIQUID | 100 | 1 | |
| 70970-100-02 | OHTrust Nano Ion Water | 1 in 1 PACKAGE | LIQUID | 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 32460e24-386c-4b03-9a6a-9118cc66fdb4 | 446842b8-c2cb-496f-a102-2fd6a4474e7d | 2016-09-26 | Warnings | 32460e24-386c-4b03-9a6a-9118cc66fdb4 446842b8-c2cb-496f-a102-2fd6a4474e7d | ||
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.