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.
N-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
- N-13
- Generic name
- CEANOTHUS AMERICANUS LEAF, URTICA URENS, SODIUM CHLORIDE, LACHESIS MUTA WHOLE, CINCHONA OFFICINALIS BARK, LYCOPODIUM CLAVATUM WHOLE, FERRIC CHLORIDE HEXAHYDRATE, AND SUS SCROFA SPLEEN
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 146c5465-bcd9-4057-8975-dc1088b9971b
- SPL ID
- 2b538be3-baa8-3c2b-e063-6294a90a1489
- Version
- 3
- Effective date
- 2025-01-09
- Source export date
- 2026-10-27
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/55ffdfed5c29f1b4aed512886bd3fb7831e157cc4948137779971a558752ed2b/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:07:22
| 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 | N-13 | openfda.brand_name | |
| generic name | CEANOTHUS AMERICANUS LEAF, URTICA URENS, SODIUM CHLORIDE, LACHESIS MUTA WHOLE, CINCHONA OFFICINALIS BARK, LYCOPODIUM CLAVATUM WHOLE, FERRIC CHLORIDE HEXAHYDRATE, AND SUS SCROFA SPLEEN | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0211-1 | openfda.package_ndc |
| ndc | product | 58264-0211 | openfda.product_ndc |
| ndc11 | package | 58264021101 | derived:openfda.package_ndc |
| spl id | 2b538be3-baa8-3c2b-e063-6294a90a1489 | id | |
| spl set id | 146c5465-bcd9-4057-8975-dc1088b9971b | set_id | |
| unii | 005ICF6L27 | openfda.unii | |
| unii | 451W47IQ8X | openfda.unii | |
| unii | IHN2NQ5OF9 | openfda.unii | |
| unii | 0I2XIN602U | openfda.unii | |
| unii | 92AMN5J79Y | openfda.unii | |
| unii | 25B1Y14T8N | openfda.unii | |
| unii | S003A158SB | openfda.unii | |
| unii | 6Y582I290C | 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.