warnings
Warnings
Cold Crush Adult
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
- Cold Crush Adult
- Generic name
- ACONITUM NAPELLUS, ALLIUM CEPA, BRYONIA ALBA, EUPHRASIA OFFICINALIS, GELSEMIUM SEMPERVIRENS, NUX VOMICA, PULSATILLA, RHUS TOXICODENDRON, SABADILLA
- Manufacturer
- Genexa Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 78ff93d3-5c77-b951-e053-2a91aa0adda9
- SPL ID
- 59a83a25-acaf-7b07-e063-6294a90a56d0
- Version
- 14
- Effective date
- 2026-08-22
- Source export date
- 2026-10-30
- 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/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:30:39
| 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 | Cold Crush Adult | openfda.brand_name | |
| generic name | ACONITUM NAPELLUS, ALLIUM CEPA, BRYONIA ALBA, EUPHRASIA OFFICINALIS, GELSEMIUM SEMPERVIRENS, NUX VOMICA, PULSATILLA, RHUS TOXICODENDRON, SABADILLA | openfda.generic_name | |
| manufacturer name | Genexa Inc. | openfda.manufacturer_name | |
| ndc | package | 69676-0006-3 | openfda.package_ndc |
| ndc | package | 69676-0006-1 | openfda.package_ndc |
| ndc | product | 69676-0006 | openfda.product_ndc |
| ndc11 | package | 69676000601 | derived:openfda.package_ndc |
| ndc11 | package | 69676000603 | derived:openfda.package_ndc |
| spl id | 59a83a25-acaf-7b07-e063-6294a90a56d0 | id | |
| spl set id | 78ff93d3-5c77-b951-e053-2a91aa0adda9 | set_id | |
| unii | C9642I91WL | openfda.unii | |
| unii | 269XH13919 | openfda.unii | |
| unii | 639KR60Q1Q | openfda.unii | |
| unii | 6NAF1689IO | openfda.unii | |
| unii | 492225Q21H | openfda.unii | |
| unii | 8E272251DI | openfda.unii | |
| unii | T7J046YI2B | openfda.unii | |
| unii | U0NQ8555JD | openfda.unii | |
| unii | 46PYZ1F82M | 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.