TheraBreath
- Product NDC
- 10237-274
- 11-digit product format
- 102370274
- Labeler code
- 10237
- Product ID
- 10237-274_5b11930d-111a-400e-e063-6294a90a9e6b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- KIT
- Route
- ORAL
- Labeler
- Church & Dwight Co., Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-06-01
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TheraBreath
- Listing expiration
- 2027-12-31
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 53c1086d-264b-9d00-e063-6394a90ad19d | Available on FDA.report |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 10237-274-01 | 10237027401 | 1 KIT in 1 CARTON (10237-274-01) * 473 mL in 1 BOTTLE, PLASTIC (10237-260-16) * 473 mL in 1 BOTTLE, PLASTIC | 1 kit | 2026-06-01 | No | No | Current |