warnings
Warnings If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
Crest Pro-Health Stages
- Product NDC
- 37000-675
- 11-digit product format
- 370000675
- Labeler code
- 37000
- Product ID
- 37000-675_6a986bb2-a042-13bb-e053-2991aa0a97ad
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Procter & Gamble Manufacturing Company
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2008-08-01
- Marketing end
- 2019-08-27
- Substance
- SODIUM FLUORIDE
- Active strength
- 2 mg/g
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 37000-675 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 37000-675 | 37000-675-04 | D | Discontinued by firm | 2026-07-31 |
openFDA label cross-check#
Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Plus White | SODIUM MONOFLUOROPHOSPHATE | CCA Industries, Inc. | 7581b27b-6acb-45b0-8804-b5dae3498931 | 2018-08-01 | Warnings |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.