Quercus Essence
- Product NDC
- 48951-8119
- 11-digit product format
- 489518119
- Labeler code
- 48951
- Product ID
- 48951-8119_6b15b164-0183-e215-e053-2a91aa0a98c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Quercus Essence
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- QUERCUS ROBUR WHOLE
- Active strength
- 1 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-8119-6 | Quercus Essence | 125 mL in 1 BOTTLE, GLASS | LIQUID | 125 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-8119 | QUERCUS ESSENCE LIQUID [URIEL PHARMACY INC.] | 3 | Legacy NDC, 1 package rows | 20231109_6723fa73-177b-4077-b0e0-a2890bc9864e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-8119-6 | 48951811906 | 125 mL in 1 BOTTLE, GLASS (48951-8119-6) | 125 ml | 2009-09-01 | 0000-00-00 | No | No | Current |