warnings
Stop use and ask doctor if symptoms persist more than 5 days or worsen. If pregnant or breast-feeding ask a health professional before use. Do not use more than the recommended dose. Keep out of reach of children.
GUNA HAY FEVER RELIEF
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
- GUNA HAY FEVER RELIEF
- Generic name
- STRYCHNOS NUX VOMICA SEED - HISTAMINE DIHYDROCHLORIDE - MANGANESE - SCHOENOCAULON OFFICINALE SEED - APIS MELLIFERA - ARSENIC TRIOXIDE - SILVER NITRATE - ONION - EUPHRASIA STRICTA - GALPHIMIA GLAUCA FLOWERING TOP - SULFUR -
- Manufacturer
- Guna spa
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b8db4fc6-f235-6f2b-e053-2a95a90a186f
- SPL ID
- d3322d60-dd44-8e96-e053-2995a90a54b0
- Version
- 3
- Effective date
- 2021-12-15
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:19:34
| 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 | GUNA HAY FEVER RELIEF | openfda.brand_name | |
| generic name | STRYCHNOS NUX VOMICA SEED - HISTAMINE DIHYDROCHLORIDE - MANGANESE - SCHOENOCAULON OFFICINALE SEED - APIS MELLIFERA - ARSENIC TRIOXIDE - SILVER NITRATE - ONION - EUPHRASIA STRICTA - GALPHIMIA GLAUCA FLOWERING TOP - SULFUR - | openfda.generic_name | |
| manufacturer name | Guna spa | openfda.manufacturer_name | |
| ndc | package | 17089-476-21 | openfda.package_ndc |
| ndc | package | 17089-476-20 | openfda.package_ndc |
| ndc | product | 17089-476 | openfda.product_ndc |
| ndc11 | package | 17089047620 | derived:openfda.package_ndc |
| ndc11 | package | 17089047621 | derived:openfda.package_ndc |
| spl id | d3322d60-dd44-8e96-e053-2995a90a54b0 | id | |
| spl set id | b8db4fc6-f235-6f2b-e053-2a95a90a186f | set_id | |
| unii | C9642I91WL | openfda.unii | |
| unii | 269XH13919 | openfda.unii | |
| unii | 3POA0Q644U | openfda.unii | |
| unii | 93PH5Q8M7E | openfda.unii | |
| unii | 42Z2K6ZL8P | openfda.unii | |
| unii | 95IT3W8JZE | openfda.unii | |
| unii | S7V92P67HO | openfda.unii | |
| unii | 6NAF1689IO | openfda.unii | |
| unii | 492225Q21H | openfda.unii | |
| unii | 70FD1KFU70 | openfda.unii | |
| unii | 7S82P3R43Z | 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.