warnings
Warnings: Use Only as directed. Stop use and ask a doctor if symptoms worsen or do not improve after 5 days.
Allergena Texas Cedar Fever
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
- Allergena Texas Cedar Fever
- Generic name
- ECHINACEA,BAPTISIA TINCTORIA, HYDRASTIS CANADENSIS, MYRRHA, NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, TRIGONELLA FOENUM-GRAECUM, TEXAS TREE, TEXAS WEED, TEXAS GRASS
- Manufacturer
- Meditrend, Inc. DBA Progena Professional Formulations
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 276741f2-a2fc-4e5f-bdc9-85b88eb7c22e
- SPL ID
- 2a97343a-9a5e-e604-e063-6394a90af65c
- Version
- 2
- Effective date
- 2024-12-31
- Source export date
- 2026-10-27
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:45:29
| 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 | Allergena Texas Cedar Fever | openfda.brand_name | |
| generic name | ECHINACEA,BAPTISIA TINCTORIA, HYDRASTIS CANADENSIS, MYRRHA, NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, TRIGONELLA FOENUM-GRAECUM, TEXAS TREE, TEXAS WEED, TEXAS GRASS | openfda.generic_name | |
| manufacturer name | Meditrend, Inc. DBA Progena Professional Formulations | openfda.manufacturer_name | |
| ndc | package | 62713-969-01 | openfda.package_ndc |
| ndc | product | 62713-969 | openfda.product_ndc |
| ndc11 | package | 62713096901 | derived:openfda.package_ndc |
| spl id | 2a97343a-9a5e-e604-e063-6394a90af65c | id | |
| spl set id | 276741f2-a2fc-4e5f-bdc9-85b88eb7c22e | set_id | |
| unii | 294L626TT0 | openfda.unii | |
| unii | A7IKY24TR7 | openfda.unii | |
| unii | WIB701MW2H | openfda.unii | |
| unii | Z4Y9ZSV4KK | openfda.unii | |
| unii | 3538FNV8AY | openfda.unii | |
| unii | 577VA5B4HP | openfda.unii | |
| unii | 232DMH0XVF | openfda.unii | |
| unii | KPO1Z9N98A | openfda.unii | |
| unii | O12H03B41R | openfda.unii | |
| unii | 95447163DG | openfda.unii | |
| unii | 11E6VI8VEG | openfda.unii | |
| unii | JQ5HI5004M | openfda.unii | |
| unii | 2A64U81OQ3 | openfda.unii | |
| unii | 476DVV63WP | openfda.unii | |
| unii | 17Q05812N1 | openfda.unii | |
| unii | 605T96G8Y5 | openfda.unii | |
| unii | 34X886W1H4 | openfda.unii | |
| unii | VU8C8SB23P | openfda.unii | |
| unii | V174354MDI | openfda.unii | |
| unii | 5928LJ1441 | openfda.unii | |
| unii | 83X1I1RR5F | openfda.unii | |
| unii | 07A108ZKW5 | openfda.unii | |
| unii | KU1V1898XX | openfda.unii | |
| unii | 5Q246DS5BS | openfda.unii | |
| unii | PY0JA16R2G | openfda.unii | |
| unii | 83N78IDA7P | openfda.unii | |
| unii | 1GH3WV23KH | openfda.unii | |
| unii | HU8V6E7HOA | openfda.unii | |
| unii | G684LX721Q | openfda.unii | |
| unii | 766QT72BK6 | openfda.unii | |
| unii | 098LKX5NCN | openfda.unii | |
| unii | P6K070AR8V | 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.