warnings
Warnings If symptoms worsen or persist for more than 7 days consult a physician. If pregnant or breastfeeding consult a physician before use. Keep out of reach of children.
Triple Allergy Defense
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
- Triple Allergy Defense
- Generic name
- ALLIUM CEPA, AMBROSIA ARTEMISIIFOLIA, EUPHRASIA OFFICINALIS, GALPHIMIA GLAUCA, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, LEMNA MINOR, LUFFA OPERCULATA, NATRUM MURIATICUM, POLYPORUS PINICOLA, SABADILLA
- Manufacturer
- Nenningers Naturals, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e1459ef4-6980-4b2b-94c1-6c896a9cb6bd
- SPL ID
- 46cb268e-dd0d-9340-e063-6294a90ad93b
- Version
- 8
- Effective date
- 2025-12-25
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:56:01
| 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 | Triple Allergy Defense | openfda.brand_name | |
| generic name | ALLIUM CEPA, AMBROSIA ARTEMISIIFOLIA, EUPHRASIA OFFICINALIS, GALPHIMIA GLAUCA, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, LEMNA MINOR, LUFFA OPERCULATA, NATRUM MURIATICUM, POLYPORUS PINICOLA, SABADILLA | openfda.generic_name | |
| manufacturer name | Nenningers Naturals, LLC | openfda.manufacturer_name | |
| ndc | package | 42731-033-02 | openfda.package_ndc |
| ndc | product | 42731-033 | openfda.product_ndc |
| ndc11 | package | 42731003302 | derived:openfda.package_ndc |
| spl id | 46cb268e-dd0d-9340-e063-6294a90ad93b | id | |
| spl set id | e1459ef4-6980-4b2b-94c1-6c896a9cb6bd | set_id | |
| unii | C9642I91WL | openfda.unii | |
| unii | 3POA0Q644U | openfda.unii | |
| unii | 8P2VLG2456 | openfda.unii | |
| unii | R763EBH88T | openfda.unii | |
| unii | 93PH5Q8M7E | openfda.unii | |
| unii | 621HHM46SV | openfda.unii | |
| unii | 30D02U2IRN | openfda.unii | |
| unii | 451W47IQ8X | openfda.unii | |
| unii | C4MO6809HU | openfda.unii | |
| unii | 9W34L2CQ9A | openfda.unii | |
| unii | 6NAF1689IO | 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.