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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| Genexa Kids Calm Keeper | ACONITUM NAPELLUS, CALCAREA PHOSPHORICA, CHAMOMILLA, GELSEMIUM SEPERVIRENS, IGNATIA AMARA, KALI CARBONICUM, PASSIFLORA INCARNATA, VALERIANA OFFICINALIS | Genexa Inc. | ba5de524-dac6-8b54-e053-2995a90ac6ef | 2025-11-25 | Warnings | 91D9GV0Z28 |
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| DOCTRUST ONE S Tooth | SODIUM FLUORIDE, DENTAL TYPE SILICA, POTASSIUM NIRATE | DONG IL PHARMS CO.,LTD | 4476923a-48f1-9f72-e063-6394a90a0708 | 2025-11-25 | Warnings | ETJ7Z6XBU4 RU45X2JN0Z |
| DOCTRUST K Tooth | SILICON DIOXIDE, SODIUM MONOFLUOROPHOSPHATE | DONG IL PHARMS CO.,LTD | 44768dd1-b132-c33b-e063-6294a90accd4 | 2025-11-25 | Warnings | ETJ7Z6XBU4 |
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| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | beda35c3-9a8b-47ad-e053-2995a90a7b1b | 2025-11-24 | Warnings | 059QF0KO0R |
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| ULINE Eyewash | EYEWASH | Niagara Pharmaceuticals Inc. | 2d7f22d2-320b-6af1-e063-6294a90addc6 | 2025-11-24 | Warnings | 059QF0KO0R |
| Pur-Wash | EYEWASH | Niagara Pharmaceuticals, Inc. | 0d43b1c1-2699-37f1-e054-00144ff88e88 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 777e1559-786f-8d54-e053-2991aa0aa98d | 2025-11-24 | Warnings | 059QF0KO0R |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.