D-120
- Product NDC
- 58264-0126
- 11-digit product format
- 582640126
- Labeler code
- 58264
- Product ID
- 58264-0126_2b9ef26a-132d-fdee-e063-6394a90abb13
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcium fluoride, Bismuth Subnitrate, Zinc, Mercuric Chloride, Toxicodendron pubescens leaf, Antimony trisulfide, Barium carbonate, Echinacea angustifolia, Iodine, Phosphoric acid, Potassium carbonate, Dibasic potassium phosphate, and Thuja occidentalis Leafy twig
- Dosage form
- SOLUTION
- Route
- SUBLINGUAL
- Labeler
- DNA Labs, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1990-01-01
- Substance
- ANTIMONY TRISULFIDE; BARIUM CARBONATE; BISMUTH SUBNITRATE; CALCIUM FLUORIDE; DIBASIC POTASSIUM PHOSPHATE; ECHINACEA ANGUSTIFOLIA; IODINE; MERCURIC CHLORIDE; PHOSPHORIC ACID; POTASSIUM CARBONATE; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS LEAF; ZINC
- Active strength
- 8; 8; 6; 8; 4; 4; 4; 6; 4; 6; 4; 4; 8 [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; [hp_X]/mL
- Pharmacologic classes
- Bismuth [CS], Bismuth [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- D-120
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ANTIMONY TRISULFIDE | 8 [hp_X]/mL |
| BARIUM CARBONATE | 8 [hp_X]/mL |
| BISMUTH SUBNITRATE | 6 [hp_X]/mL |
| CALCIUM FLUORIDE | 8 [hp_X]/mL |
| DIBASIC POTASSIUM PHOSPHATE | 4 [hp_X]/mL |
| ECHINACEA ANGUSTIFOLIA | 4 [hp_X]/mL |
| IODINE | 4 [hp_X]/mL |
| MERCURIC CHLORIDE | 6 [hp_X]/mL |
| PHOSPHORIC ACID | 4 [hp_X]/mL |
| POTASSIUM CARBONATE | 6 [hp_X]/mL |
| THUJA OCCIDENTALIS LEAFY TWIG | 4 [hp_X]/mL |
| TOXICODENDRON PUBESCENS LEAF | 4 [hp_X]/mL |
| ZINC | 8 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F79059A38U, 6P669D8HQ8, H19J064BA5, O3B55K4YKI, CI71S98N1Z, VB06AV5US8, 9679TC07X4, 53GH7MZT1R, E4GA8884NN, BQN1B9B9HA, 1NT28V9397, 6IO182RP7A, J41CSQ7QDS |
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 |
|---|
| 58264-0126-1 | D-120 | 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 |
|---|
| 58264-0126 | D-120 (CALCIUM FLUORIDE, BISMUTH SUBNITRATE, ZINC, MERCURIC CHLORIDE, TOXICODENDRON PUBESCENS LEAF, ANTIMONY TRISULFIDE, BARIUM CARBONATE, ECHINACEA ANGUSTIFOLIA, IODINE, PHOSPHORIC ACID, POTASSIUM CARBONATE, DIBASIC POTASSIUM PHOSPHATE, AND THUJA OCCIDENTALIS LEAFY TWIG) SOLUTION [DNA LABS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250115_9525c016-f0dd-43fd-a4e9-062075107eec.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58264-0126-1 | 58264012601 | 29.57 mL in 1 BOTTLE, GLASS (58264-0126-1) | 29.57 ml | 1990-01-01 | 0000-00-00 | No | No | Current |