N-14
- Product NDC
- 58264-0212
- 11-digit product format
- 582640212
- Labeler code
- 58264
- Product ID
- 58264-0212_2b539e1c-6623-f6dc-e063-6294a90a587d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fucus vesiculosus, Sodium chloride, Lycopus virginicus, Spongia officinalis skeleton, roasted, Potassium iodide, Calcium iodide, Thyroid, Unspecified, Bos taurus adrenal gland, Bos Taurus Pituitary Gland, Posterior, Bos taurus thymus, and Sus scrofa spleen
- Dosage form
- SOLUTION
- Route
- SUBLINGUAL
- Labeler
- DNA Labs, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1990-01-01
- Substance
- BOS TAURUS ADRENAL GLAND; BOS TAURUS PITUITARY GLAND, POSTERIOR; BOS TAURUS THYMUS; CALCIUM IODIDE; FUCUS VESICULOSUS; LYCOPUS VIRGINICUS; POTASSIUM IODIDE; SODIUM CHLORIDE; SPONGIA OFFICINALIS SKELETON, ROASTED; SUS SCROFA SPLEEN; THYROID, UNSPECIFIED
- Active strength
- 200; 200; 200; 6; 4; 6; 6; 6; 4; 200; 200 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- N-14
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BOS TAURUS ADRENAL GLAND | 200 [hp_X]/mL |
| BOS TAURUS PITUITARY GLAND, POSTERIOR | 200 [hp_X]/mL |
| BOS TAURUS THYMUS | 200 [hp_X]/mL |
| CALCIUM IODIDE | 6 [hp_X]/mL |
| FUCUS VESICULOSUS | 4 [hp_X]/mL |
| LYCOPUS VIRGINICUS | 6 [hp_X]/mL |
| POTASSIUM IODIDE | 6 [hp_X]/mL |
| SODIUM CHLORIDE | 6 [hp_X]/mL |
| SPONGIA OFFICINALIS SKELETON, ROASTED | 4 [hp_X]/mL |
| SUS SCROFA SPLEEN | 200 [hp_X]/mL |
| THYROID, UNSPECIFIED | 200 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | M2776SWB29, 7JM57I419K, 8XEJ88V2T8, 8EKI9QEE2H, 535G2ABX9M, TWH5125Q6F, 1C4QK22F9J, 451W47IQ8X, 1PIP394IID, 92AMN5J79Y, 0B4FDL9I6P |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 58264-0212-1 | N-14 | 29.57 mL in 1 BOTTLE, GLASS | SOLUTION | 29.57 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58264-0212 | N-14 (FUCUS VESICULOSUS, SODIUM CHLORIDE, LYCOPUS VIRGINICUS, SPONGIA OFFICINALIS SKELETON, ROASTED, POTASSIUM IODIDE, CALCIUM IODIDE, THYROID, UNSPECIFIED, BOS TAURUS ADRENAL GLAND, BOS TAURUS PITUITARY GLAND, POSTERIOR, BOS TAURUS THYMUS, AND SUS SCROFA SPLEEN) SOLUTION [DNA LABS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250112_3d64739c-5d61-4e88-8612-d5f6994f1c3c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58264-0212-1 | 58264021201 | 29.57 mL in 1 BOTTLE, GLASS (58264-0212-1) | 29.57 ml | 1990-01-01 | 0000-00-00 | No | No | Current |