warnings
Warnings: For external use only. Avoid contact with eyes. Do not ingest. Keep out of reach from children 2 years of age and younger.
Natural Seal Itch Relief for 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
- Natural Seal Itch Relief for Kids
- Generic name
- LIDOCAINE
- Manufacturer
- Kericure Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 31cc0c95-5864-4737-b085-8f58e00f4f05
- SPL ID
- 4a8fcd47-eefa-4d7e-9c56-9a81c5711546
- Version
- 2
- Effective date
- 2024-12-12
- 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 05:53:53
| Harmonized routes |
|---|
| TOPICAL |
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 |
|---|---|---|---|
| application number | M017 | openfda.application_number | |
| brand name | Natural Seal Itch Relief for Kids | openfda.brand_name | |
| generic name | LIDOCAINE | openfda.generic_name | |
| manufacturer name | Kericure Inc. | openfda.manufacturer_name | |
| ndc | package | 78280-712-10 | openfda.package_ndc |
| ndc | product | 78280-712 | openfda.product_ndc |
| ndc11 | package | 78280071210 | derived:openfda.package_ndc |
| rxcui | 1549223 | openfda.rxcui | |
| spl id | 4a8fcd47-eefa-4d7e-9c56-9a81c5711546 | id | |
| spl set id | 31cc0c95-5864-4737-b085-8f58e00f4f05 | set_id | |
| unii | 98PI200987 | 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.