DenTek Eugenol
- Product NDC
- 67659-400
- 11-digit product format
- 676590400
- Labeler code
- 67659
- Product ID
- 67659-400_e4f87bd3-2593-5603-e053-2a95a90a5e6e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Eugenol
- Dosage form
- LIQUID
- Route
- DENTAL
- Labeler
- Team Technologies, Inc
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-07-01
- Marketing end
- 0000-00-00
- Substance
- EUGENOL
- Active strength
- 850 mg/mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67659-400-20 | DenTek Eugenol | 3.5 mL in 1 VIAL, GLASS | LIQUID | 3.5 | | 3 |
| 67659-400-21 | DenTek Eugenol | 1 in 1 KIT | LIQUID | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67659-400 | DENTEK EUGENOL (EUGENOL) LIQUID [TEAM TECHNOLOGIES, INC] | 3 | Legacy NDC, 2 package rows | 20220802_3afcd2bf-94fb-11c9-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67659-400-20 | 67659040020 | 3.5 mL in 1 VIAL, GLASS | 3.5 ml | | | | | Historical |
| 67659-400-21 | 67659040021 | 1 VIAL, GLASS in 1 KIT (67659-400-21) > 3.5 mL in 1 VIAL, GLASS (67659-400-20) | | 2015-07-01 | 0000-00-00 | No | No | Current |