warnings
Warnings Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
ACT Kids Berry Blast
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
- ACT Kids Berry Blast
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Chattem, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4f81ea98-5c74-4473-9764-3f11d627cdf1
- SPL ID
- e74290ff-fedb-4273-8c34-d2b044cbd452
- Version
- 1
- Effective date
- 2026-02-01
- 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 05:35:23
| 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 |
|---|---|---|---|
| application number | M021 | openfda.application_number | |
| brand name | ACT Kids Berry Blast | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Chattem, Inc. | openfda.manufacturer_name | |
| ndc | package | 41167-0976-0 | openfda.package_ndc |
| ndc | product | 41167-0976 | openfda.product_ndc |
| ndc11 | package | 41167097600 | derived:openfda.package_ndc |
| rxcui | 240698 | openfda.rxcui | |
| spl id | e74290ff-fedb-4273-8c34-d2b044cbd452 | id | |
| spl set id | 4f81ea98-5c74-4473-9764-3f11d627cdf1 | set_id | |
| unii | 8ZYQ1474W7 | 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.