warnings
Warnings Use only if cap seal is unbroken. As with drugs if you are pregnant or nursing a baby seek professional advice before using this product. Keep this and all medication out of the reach of children.
AM-13
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-13
- Generic name
- CARBON DISULFIDE, SILVER NITRATE, CORALLIUM RUBRUM WHOLE, CUPRIC ARSENITE, ASIAN GINSENG, HYPERICUM PERFORATUM, LATHYRUS SATIVUS WHOLE, PICRIC ACID, SELENIUM, DATURA STRAMONIUM WHOLE, AND ZINC
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 735d1d54-dd9d-4867-bfdf-3003d7403953
- SPL ID
- 2b530d94-bb57-3c78-e063-6294a90a8ec5
- Version
- 3
- Effective date
- 2025-01-09
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:19:30
| 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-13 | openfda.brand_name | |
| generic name | CARBON DISULFIDE, SILVER NITRATE, CORALLIUM RUBRUM WHOLE, CUPRIC ARSENITE, ASIAN GINSENG, HYPERICUM PERFORATUM, LATHYRUS SATIVUS WHOLE, PICRIC ACID, SELENIUM, DATURA STRAMONIUM WHOLE, AND ZINC | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0352-1 | openfda.package_ndc |
| ndc | product | 58264-0352 | openfda.product_ndc |
| ndc11 | package | 58264035201 | derived:openfda.package_ndc |
| spl id | 2b530d94-bb57-3c78-e063-6294a90a8ec5 | id | |
| spl set id | 735d1d54-dd9d-4867-bfdf-3003d7403953 | set_id | |
| unii | FI8B4CLS9I | openfda.unii | |
| unii | SK8L60BCSQ | openfda.unii | |
| unii | XK4IUX8MNB | openfda.unii | |
| unii | CUQ3A77YXI | openfda.unii | |
| unii | S54S8B99E8 | openfda.unii | |
| unii | 95IT3W8JZE | openfda.unii | |
| unii | MX7553JF12 | openfda.unii | |
| unii | A49OS0F91S | openfda.unii | |
| unii | 22Z32PWR7R | openfda.unii | |
| unii | J41CSQ7QDS | openfda.unii | |
| unii | H6241UJ22B | 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.