warnings
Warnings Use only if cap seal is unbroken. If pregnant or breastfeeding, ask a healthcare professional before use. Keep this and all medication out of the reach of children.
AM-7
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- AM-7
- Generic name
- STRYCHNOS NUX-VOMICA SEED, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, AND BUFO BUFO WHOLE
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c913d2ca-dd24-4139-b61b-2c1d267cc4e8
- SPL ID
- 2b530979-bfa8-24b5-e063-6394a90a76eb
- Version
- 3
- Effective date
- 2025-01-09
- Source export date
- 2026-11-06
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:03:55
| Harmonized routes |
|---|
| SUBLINGUAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | AM-7 | openfda.brand_name | |
| generic name | STRYCHNOS NUX-VOMICA SEED, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, AND BUFO BUFO WHOLE | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0346-1 | openfda.package_ndc |
| ndc | product | 58264-0346 | openfda.product_ndc |
| ndc11 | package | 58264034601 | derived:openfda.package_ndc |
| spl id | 2b530979-bfa8-24b5-e063-6394a90a76eb | id | |
| spl set id | c913d2ca-dd24-4139-b61b-2c1d267cc4e8 | set_id | |
| unii | 269XH13919 | openfda.unii | |
| unii | DP1U601YQS | openfda.unii | |
| unii | 70WT22SF4B | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.