warnings
Warnings Warnings
Allday 5000 Sensitive
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
- Allday 5000 Sensitive
- Generic name
- 1.1% SODIUM FLUORIDE TOOTHPASTE
- Manufacturer
- Elevate Oral Care
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 401f5e96-095b-c001-e063-6394a90ab55e
- SPL ID
- 436963b5-15ca-c8e1-e063-6294a90ae7e4
- Version
- 2
- Effective date
- 2025-11-12
- 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 06:26:32
| Harmonized routes |
|---|
| DENTAL |
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 | Allday 5000 Sensitive | openfda.brand_name | |
| generic name | 1.1% SODIUM FLUORIDE TOOTHPASTE | openfda.generic_name | |
| manufacturer name | Elevate Oral Care | openfda.manufacturer_name | |
| ndc | package | 57511-0006-1 | openfda.package_ndc |
| ndc | product | 57511-0006 | openfda.product_ndc |
| ndc11 | package | 57511000601 | derived:openfda.package_ndc |
| rxcui | 2682752 | openfda.rxcui | |
| spl id | 436963b5-15ca-c8e1-e063-6294a90ae7e4 | id | |
| spl set id | 401f5e96-095b-c001-e063-6394a90ab55e | set_id | |
| unii | 8ZYQ1474W7 | openfda.unii | |
| unii | RU45X2JN0Z | 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.