Plantago e fol. 10 Special Order
- Product NDC
- 48951-8294
- 11-digit product format
- 489518294
- Labeler code
- 48951
- Product ID
- 48951-8294_12500c1b-6480-47e0-bfdb-80e8b97275f1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Plantago e fol. 10 Special Order
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- PLANTAGO MAJOR LEAF
- Active strength
- 1 [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 48951-8294-5 | Plantago e fol. 10 Special Order | 60 g in 1 TUBE | GEL | 60 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-8294 | PLANTAGO E FOL. 10 SPECIAL ORDER GEL [URIEL PHARMACY INC.] | 1 | Legacy NDC, 1 package rows | 20150122_791052c0-a788-428d-aa35-3edfb9250dbc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 48951-8294-5 | 48951829405 | 60 g in 1 TUBE | 60 g | Historical |