Pleo Usti
- Product NDC
- 60681-5601
- 11-digit product format
- 606815601
- Labeler code
- 60681
- Product ID
- 60681-5601_7b103d01-a1ae-49ed-8698-46d8227a5bd8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ustilago maydis
- Dosage form
- SOLUTION/ DROPS
- Route
- ORAL
- Labeler
- Sanum Kehlbeck GmbH & Co. KG
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1998-08-19
- Marketing end
- 0000-00-00
- Substance
- USTILAGO MAYDIS
- Active strength
- 5 [hp_X]/10mL
- 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 |
|---|
| 60681-5601-1 | Pleo Usti | 30 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 30 | | 2 |
| 60681-5601-1 | Pleo Usti | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60681-5601 | PLEO USTI (USTILAGO MAYDIS) SOLUTION/ DROPS [SANUM KEHLBECK GMBH & CO. KG] | 2 | Legacy NDC, 2 package rows | 20110114_4c5bdb24-162f-4a6e-8d6f-c8be516ba9bb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 60681-5601-1 | 60681560101 | 30 mL in 1 BOTTLE, DROPPER | 30 ml | Historical |