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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.