AM-7
- Product NDC
- 58264-0346
- 11-digit product format
- 582640346
- Labeler code
- 58264
- Product ID
- 58264-0346_2b530979-bfa8-24b5-e063-6394a90a76eb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Strychnos nux-vomica seed, Sodium Phosphate, Dibasic, Heptahydrate, and BUFO BUFO WHOLE
- Dosage form
- SOLUTION
- Route
- SUBLINGUAL
- Labeler
- DNA Labs, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1990-01-01
- Substance
- BUFO BUFO WHOLE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; STRYCHNOS NUX-VOMICA SEED
- Active strength
- 12; 8; 8 [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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| DP1U601YQS | BUFO BUFO WHOLE | | BUFO BUFO WHOLE |
| 70WT22SF4B | SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE | 7782-85-6 | SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE |
| 269XH13919 | STRYCHNOS NUX-VOMICA SEED | 8046-97-7 | STRYCHNOS NUX-VOMICA SEED |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 58264-0346-1 | 58264034601 | 29.57 mL in 1 BOTTLE, GLASS (58264-0346-1) | 29.57 ml | 1990-01-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| AM-7 | DNA Labs, Inc. | 2025-01-09 | HUMAN OTC DRUG LABEL | 3 |