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.
N-8
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-8
- Generic name
- SILICON DIOXIDE, ATROPA BELLADONNA, CITRULLUS COLOCYNTHIS FRUIT PULP, BLACK COHOSH, ANEMONE PULSATILLA, SEPIA OFFICINALIS JUICE, PALLADIUM, APIS MELLIFERA, AND BOS TAURUS OVARY
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c25cdcb5-9469-48bb-b216-0a9d8d644e12
- SPL ID
- 2b535a39-0bac-b8c0-e063-6394a90a80d3
- Version
- 4
- Effective date
- 2025-01-09
- Source export date
- 2026-10-12
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:44:52
| 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-8 | openfda.brand_name | |
| generic name | SILICON DIOXIDE, ATROPA BELLADONNA, CITRULLUS COLOCYNTHIS FRUIT PULP, BLACK COHOSH, ANEMONE PULSATILLA, SEPIA OFFICINALIS JUICE, PALLADIUM, APIS MELLIFERA, AND BOS TAURUS OVARY | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0206-1 | openfda.package_ndc |
| ndc | product | 58264-0206 | openfda.product_ndc |
| ndc11 | package | 58264020601 | derived:openfda.package_ndc |
| spl id | 2b535a39-0bac-b8c0-e063-6394a90a80d3 | id | |
| spl set id | c25cdcb5-9469-48bb-b216-0a9d8d644e12 | set_id | |
| unii | 5TWQ1V240M | openfda.unii | |
| unii | QDL83WN8C2 | openfda.unii | |
| unii | 66LZN1C747 | openfda.unii | |
| unii | ETJ7Z6XBU4 | openfda.unii | |
| unii | WQZ3G9PF0H | openfda.unii | |
| unii | 7S82P3R43Z | openfda.unii | |
| unii | I76KB35JEV | openfda.unii | |
| unii | K73E24S6X9 | openfda.unii | |
| unii | 23H32AOH17 | 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.