warnings
Warnings For oral (sublingual) use. Keep out of reach of children. Recommended for children ages 3 to 12. Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.
Allergy Kids
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
- Allergy Kids
- Generic name
- URTICA DIOICA LEAF, INULA HELENIUM ROOT, ANGELICA ARCHANGELICA ROOT, PINE NEEDLE OIL (PINUS SYLVESTRIS), SODIUM CHLORIDE, AND ALTHAEA OFFICINALIS ROOT
- Manufacturer
- Forces of Nature
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4886109c-dd7d-40c0-911f-5f12343d8e63
- SPL ID
- 4b44cda7-efb6-ef0b-e063-6294a90aba1c
- Version
- 2
- Effective date
- 2026-02-20
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:28:14
| Harmonized routes |
|---|
| SUBLINGUAL |
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 | Allergy Kids | openfda.brand_name | |
| generic name | URTICA DIOICA LEAF, INULA HELENIUM ROOT, ANGELICA ARCHANGELICA ROOT, PINE NEEDLE OIL (PINUS SYLVESTRIS), SODIUM CHLORIDE, AND ALTHAEA OFFICINALIS ROOT | openfda.generic_name | |
| manufacturer name | Forces of Nature | openfda.manufacturer_name | |
| ndc | package | 51393-5008-1 | openfda.package_ndc |
| ndc | product | 51393-5008 | openfda.product_ndc |
| ndc11 | package | 51393500801 | derived:openfda.package_ndc |
| spl id | 4b44cda7-efb6-ef0b-e063-6294a90aba1c | id | |
| spl set id | 4886109c-dd7d-40c0-911f-5f12343d8e63 | set_id | |
| unii | E55SMD6DA8 | openfda.unii | |
| unii | 451W47IQ8X | openfda.unii | |
| unii | 5EXL5H740Y | openfda.unii | |
| unii | DTN01M69SN | openfda.unii | |
| unii | TRW2FUF47H | openfda.unii | |
| unii | X6M0DRN46Q | 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.