LYCOPODIUM CLAVATUM
- Product NDC
- 10191-2034
- 11-digit product format
- 101912034
- Labeler code
- 10191
- Product ID
- 10191-2034_a47a3b8c-fe3d-47d6-9601-9d57b9b8cf6f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CLUBMOSS
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- REMEDY MAKERS
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2003-05-07
- Marketing end
- 0000-00-00
- Substance
- LYCOPODIUM CLAVATUM SPORE
- Active strength
- 9 [hp_C]/1
- 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 |
|---|
| 10191-2034-2 | LYCOPODIUM CLAVATUM | 138 in 1 VIAL, GLASS | PELLET | 138 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10191-2034 | LYCOPODIUM CLAVATUM (CLUBMOSS) PELLET [REMEDY MAKERS] | 1 | Legacy NDC, 1 package rows | 20111118_7f84926d-adb2-4312-9038-1f56551350fc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10191-2034-2 | 10191203402 | 138 in 1 VIAL, GLASS | Historical |