NDC 70602-006-01 - Exoden 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
- 70602-006
- Requested NDC
- 70602-006-01
- Package NDCs from labels
- 70602-006-01, 70602-006-02
- Manufacturer
- LIFEON Corp. | Korea Life Science Co.,ltd
- Effective date
- 2021-03-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SORBITOL SOLUTION - LIFEON Corp. | Korea Life Science Co.,ltd | LIFEON Corp. | Korea Life Science Co.,ltd | 2021-03-11 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70602-006-02 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-ae67-d8a0-e053-dadaa90a6e4e | 70602-006_Exoden Sensitive Toothpaste |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70602-006-01 | Exoden Sensitive | 120 g in 1 TUBE | PASTE | 120 | 1 | |
| 70602-006-02 | Exoden Sensitive | 1 in 1 CARTON | PASTE | 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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.