warnings
Warnings: Consult your health care provider if symptoms persist more than 5 days or worsen.
Argentum Quartz 6X
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
- Argentum Quartz 6X
- Generic name
- ARGENTUM QUARTZ 6X
- Manufacturer
- True Botanica, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1acadf89-d222-9e16-e063-6294a90a80bc
- SPL ID
- 1acae67c-8f57-feff-e063-6294a90a2bf8
- Version
- 1
- Effective date
- 2024-06-26
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:47:58
| Harmonized routes |
|---|
| ORAL |
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 | Argentum Quartz 6X | openfda.brand_name | |
| generic name | ARGENTUM QUARTZ 6X | openfda.generic_name | |
| manufacturer name | True Botanica, LLC | openfda.manufacturer_name | |
| ndc | package | 53645-1342-6 | openfda.package_ndc |
| ndc | product | 53645-1342 | openfda.product_ndc |
| ndc11 | package | 53645134206 | derived:openfda.package_ndc |
| spl id | 1acae67c-8f57-feff-e063-6294a90a2bf8 | id | |
| spl set id | 1acadf89-d222-9e16-e063-6294a90a80bc | set_id | |
| unii | 3M4G523W1G | openfda.unii | |
| unii | ETJ7Z6XBU4 | 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.