D-139
- Product NDC
- 58264-0147
- 11-digit product format
- 582640147
- Labeler code
- 58264
- Product ID
- 58264-0147_e0bb8cb3-59fc-3cfe-e053-2a95a90af040
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ARSENIC TRIOXIDE, ATROPA BELLADONNA, ACTIVATED CHARCOAL, FERROSOFERRIC PHOSPHATE, GOLDENSEAL, LYCOPODIUM CLAVATUM SPORE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, STRYCHNOS NUX-VOMICA SEED, Phosphorus, and ANEMONE PRATENSIS
- Dosage form
- SOLUTION
- Route
- SUBLINGUAL
- Labeler
- DNA Labs, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1990-01-01
- Marketing end
- 0000-00-00
- Substance
- ACTIVATED CHARCOAL; ANEMONE PRATENSIS; ARSENIC TRIOXIDE; ATROPA BELLADONNA; FERROSOFERRIC PHOSPHATE; GOLDENSEAL; LYCOPODIUM CLAVATUM SPORE; PHOSPHORUS; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; STRYCHNOS NUX-VOMICA SEED
- Active strength
- 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
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58264-0147-1 | 58264014701 | 29.57 mL in 1 BOTTLE, GLASS (58264-0147-1) | 29.57 ml | 1990-01-01 | 0000-00-00 | No | No | Current |