NDC 51270-112-01 - Hesol Rim Tonic
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
- 51270-112
- Requested NDC
- 51270-112-01
- Package NDCs from labels
- 51270-112-01, 51270-112-02
- Manufacturer
- Ecomine Co Ltd
- Effective date
- 2010-10-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hesol Rim Tonic - Ecomine Co Ltd | Ecomine Co Ltd | 2010-10-01 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 51270-112-02 | 2019-10-29 | C162847 | 48780-1 | 960f7f55-d166-8e05-e053-dbdaa90a074a | Ecomine Co Ltd |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51270-112-01 | Hesol Rim Tonic | 100 mL in 1 BOTTLE | LIQUID | 100 | 1 | |
| 51270-112-02 | Hesol Rim Tonic | 1 in 1 BOX | LIQUID | 1 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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.