Plantago 1X
- Product NDC
- 69152-1562
- 11-digit product format
- 691521562
- Labeler code
- 69152
- Product ID
- 69152-1562_1710cf39-68fa-61a4-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Plantago
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Paramesh Banerji Life Sciences LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-05-27
- Marketing end
- 0000-00-00
- Substance
- PLANTAGO MAJOR
- Active strength
- 1 [hp_X]/8mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 69152-1562-1 | Plantago 1X | 8 mL in 1 BOTTLE, DROPPER | LIQUID | 8 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69152-1562 | PLANTAGO 1X (PLANTAGO) LIQUID [PARAMESH BANERJI LIFE SCIENCES LLC] | 1 | Legacy NDC, 1 package rows | 20150527_1710cf39-68f9-61a4-e054-00144ff88e88.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 69152-1562-1 | 69152156201 | 8 mL in 1 BOTTLE, DROPPER | 8 ml | Historical |