warnings
Warnings : Use only as directed. Stop use and consult a doctor if symptoms worsen or do not improve after 5 days. If pregnant or breast-feeding, ask a health professional before use. Keep out of the reach of children.
Cedar X Formula
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
- Cedar X Formula
- Generic name
- OLIBANUM, THUJA OCCIDENTALIS, GELSEMIUM SEMPERVIRENS, ALLIUM CEPA, ANTIMONIUM TARTARICUM, HEPAR SULPHURIS CALCAREUM, JUNIPERUS COMMUNIS.
- Manufacturer
- Integrative Healing Institute, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 8ab87e13-99ad-4b25-a0c3-e46a868cc684
- SPL ID
- 4161c4fe-abe4-30ef-e063-6294a90aa911
- Version
- 6
- Effective date
- 2025-10-17
- Source export date
- 2026-10-27
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/eeb012fd0992efa4f76b2aef09dd5f84150b96392c46717c44deabcc4e3581c1/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:40:50
| 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 | Cedar X Formula | openfda.brand_name | |
| generic name | OLIBANUM, THUJA OCCIDENTALIS, GELSEMIUM SEMPERVIRENS, ALLIUM CEPA, ANTIMONIUM TARTARICUM, HEPAR SULPHURIS CALCAREUM, JUNIPERUS COMMUNIS. | openfda.generic_name | |
| manufacturer name | Integrative Healing Institute, LLC | openfda.manufacturer_name | |
| ndc | package | 59623-006-01 | openfda.package_ndc |
| ndc | package | 59623-006-02 | openfda.package_ndc |
| ndc | product | 59623-006 | openfda.product_ndc |
| ndc11 | package | 59623000601 | derived:openfda.package_ndc |
| ndc11 | package | 59623000602 | derived:openfda.package_ndc |
| spl id | 4161c4fe-abe4-30ef-e063-6294a90aa911 | id | |
| spl set id | 8ab87e13-99ad-4b25-a0c3-e46a868cc684 | set_id | |
| unii | 1NT28V9397 | openfda.unii | |
| unii | 639KR60Q1Q | openfda.unii | |
| unii | DL6OZ476V3 | openfda.unii | |
| unii | R9XLF1R1WM | openfda.unii | |
| unii | 492225Q21H | openfda.unii | |
| unii | O84B5194RL | openfda.unii | |
| unii | 1MBW07J51Q | 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.