Spongilla lacustris MT
- Product NDC
- 66096-749
- 11-digit product format
- 660960749
- Labeler code
- 66096
- Product ID
- 66096-749_d449d3d9-49bd-2a4b-e053-2995a90a5a95
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Spongilla lacustris
- Dosage form
- TINCTURE
- Route
- ORAL
- Labeler
- OHM PHARMA INC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2019-03-01
- Substance
- SPONGILLA LACUSTRIS
- Active strength
- 1 [hp_X]/.25L
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Spongilla lacustris MT
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SPONGILLA LACUSTRIS | 1 [hp_X]/.25L |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6SZ0G98BHM |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66096-749-08 | Spongilla lacustris MT | 0.25 L in 1 BOTTLE | TINCTURE | 0.25 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66096-749 | SPONGILLA LACUSTRIS MT (SPONGILLA LACUSTRIS) TINCTURE [OHM PHARMA INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20211230_a855d4ca-52ed-4e69-93b5-7304bcc84f73.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66096-749-08 | 66096074908 | .25 L in 1 BOTTLE (66096-749-08) | 2019-03-01 | 0000-00-00 | No | No | Current |