AM-14
- Product NDC
- 58264-0353
- 11-digit product format
- 582640353
- Labeler code
- 58264
- Product ID
- 58264-0353_2b530979-bfa9-24b5-e063-6394a90a76eb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SILVER, CALCIUM IODIDE, LYTTA VESICATORIA, COPPER, FERROUS IODIDE, GOLDENSEAL, IODINE, DAPHNE MEZEREUM BARK, PHOSPHORIC ACID, Phosphorus, TOXICODENDRON PUBESCENS LEAF, and RUMEX CRISPUS WHOLE
- Dosage form
- SOLUTION
- Route
- SUBLINGUAL
- Labeler
- DNA Labs, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1990-01-01
- Substance
- CALCIUM IODIDE; COPPER; DAPHNE MEZEREUM BARK; FERROUS IODIDE; GOLDENSEAL; IODINE; LYTTA VESICATORIA; PHOSPHORIC ACID; PHOSPHORUS; RUMEX CRISPUS WHOLE; SILVER; TOXICODENDRON PUBESCENS LEAF
- Active strength
- 8; 12; 30; 8; 6; 6; 6; 6; 30; 6; 12; 6 [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; [hp_X]/mL
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Coagulation Factor Activity [PE], Inhibit Ovum Fertilization [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
- AM-14
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CALCIUM IODIDE | 8 [hp_X]/mL |
| COPPER | 12 [hp_X]/mL |
| DAPHNE MEZEREUM BARK | 30 [hp_X]/mL |
| FERROUS IODIDE | 8 [hp_X]/mL |
| GOLDENSEAL | 6 [hp_X]/mL |
| IODINE | 6 [hp_X]/mL |
| LYTTA VESICATORIA | 6 [hp_X]/mL |
| PHOSPHORIC ACID | 6 [hp_X]/mL |
| PHOSPHORUS | 30 [hp_X]/mL |
| RUMEX CRISPUS WHOLE | 6 [hp_X]/mL |
| SILVER | 12 [hp_X]/mL |
| TOXICODENDRON PUBESCENS LEAF | 6 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8EKI9QEE2H, 789U1901C5, X2N6E405GV, F5452U54PN, ZW3Z11D0JV, 9679TC07X4, 3Q034RO3BT, E4GA8884NN, 27YLU75U4W, UQJ679MZAK, 3M4G523W1G, 6IO182RP7A |
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 |
|---|
| 58264-0353-1 | AM-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 |
|---|
| 58264-0353 | AM-14 (SILVER, CALCIUM IODIDE, LYTTA VESICATORIA, COPPER, FERROUS IODIDE, GOLDENSEAL, IODINE, DAPHNE MEZEREUM BARK, PHOSPHORIC ACID, PHOSPHORUS, TOXICODENDRON PUBESCENS LEAF, AND RUMEX CRISPUS WHOLE) SOLUTION [DNA LABS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250112_8bf2fde6-fd71-47f8-b5ec-c5e34857ab64.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58264-0353-1 | 58264035301 | 29.57 mL in 1 BOTTLE, GLASS (58264-0353-1) | 29.57 ml | 1990-01-01 | 0000-00-00 | No | No | Current |