warnings
Warnings If pregnant or breast-feeding, consult a health professional before use.
Allernest
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
- Allernest
- Generic name
- FORMICUM ACIDUM, LACHESIS MUTUS, LUFFA OPERCULATA. PETROLEUM, RHUS TOXICODEBDRON, ARALAI RACEMOSA,GALPHIMIA GLAUCA, THUJA OCCIDENTALIS, URTICA DICICA AND CARDIOSPERMUM
- Manufacturer
- Marco Pharma International LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 97e4b6be-f93d-43de-a881-c27970201045
- SPL ID
- 483c3446-1d4b-0503-e063-6394a90a4def
- Version
- 11
- Effective date
- 2026-01-12
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:37:11
| 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 | Allernest | openfda.brand_name | |
| generic name | FORMICUM ACIDUM, LACHESIS MUTUS, LUFFA OPERCULATA. PETROLEUM, RHUS TOXICODEBDRON, ARALAI RACEMOSA,GALPHIMIA GLAUCA, THUJA OCCIDENTALIS, URTICA DICICA AND CARDIOSPERMUM | openfda.generic_name | |
| manufacturer name | Marco Pharma International LLC. | openfda.manufacturer_name | |
| ndc | package | 60986-1003-4 | openfda.package_ndc |
| ndc | package | 60986-1003-3 | openfda.package_ndc |
| ndc | product | 60986-1003 | openfda.product_ndc |
| ndc11 | package | 60986100304 | derived:openfda.package_ndc |
| ndc11 | package | 60986100303 | derived:openfda.package_ndc |
| spl id | 483c3446-1d4b-0503-e063-6394a90a4def | id | |
| spl set id | 97e4b6be-f93d-43de-a881-c27970201045 | set_id | |
| unii | 0YIW783RG1 | openfda.unii | |
| unii | MZP2508BRR | openfda.unii | |
| unii | 93PH5Q8M7E | openfda.unii | |
| unii | 710FLW4U46 | openfda.unii | |
| unii | T90W4582DU | openfda.unii | |
| unii | 1NT28V9397 | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | C4MO6809HU | openfda.unii | |
| unii | VSW71SS07I | openfda.unii | |
| unii | 1C89KKC04E | 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.