Eugenol
- Product NDC
- 63083-1518
- 11-digit product format
- 630831518
- Labeler code
- 63083
- Product ID
- 63083-1518_0effc122-390c-41df-9e52-8e5062e0da8e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Eugenol
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Marketing end
- 0000-00-00
- Substance
- EUGENOL
- Active strength
- 9 [hp_X]/29.5mL
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63083-1518 | EUGENOL 1518 (EUGENOL) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Legacy NDC | 20220301_82b5e329-e5a9-4a05-a1d3-c122dd505d2a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-1518-1 | 63083151801 | 29.5 mL in 1 BOTTLE, DROPPER (63083-1518-1) | 29.5 ml | 1985-08-15 | 0000-00-00 | No | No | Current |