Crest Pro-Health Stages
- Product NDC
- 37000-673
- 11-digit product format
- 370000673
- Labeler code
- 37000
- Product ID
- 37000-673_9999eb27-f392-760c-e053-2a95a90ac0b7
- 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
- 2021-12-01
- 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 table| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|
| excluded product | product | 37000-673 | | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 37000-673 | 37000-673-04 | 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 table| 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 | Exact identifier |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings
Warnings If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| Sodium Fluoride | ACTIVE INGREDIENT | 8ZYQ1474W7 | CREST PRO-HEALTH STAGES (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING COMPANY] | 1 | |
| Fluoride Ion | ACTIVE MOIETY | Q80VPU408O | CREST PRO-HEALTH STAGES (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING COMPANY] | 1 | |
| carboxymethylcellulose sodium | INACTIVE INGREDIENT | K679OBS311 | CREST PRO-HEALTH STAGES (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING COMPANY] | 1 | |
| D&C red no. 28 | INACTIVE INGREDIENT | 767IP0Y5NH | CREST PRO-HEALTH STAGES (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING COMPANY] | 1 | |
| hydrated silica | INACTIVE INGREDIENT | Y6O7T4G8P9 | CREST PRO-HEALTH STAGES (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING COMPANY] | 1 | |
| saccharin sodium | INACTIVE INGREDIENT | SB8ZUX40TY | CREST PRO-HEALTH STAGES (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING COMPANY] | 1 | |
| sodium lauryl sulfate | INACTIVE INGREDIENT | 368GB5141J | CREST PRO-HEALTH STAGES (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING COMPANY] | 1 | |
| sodium phosphate | INACTIVE INGREDIENT | SE337SVY37 | CREST PRO-HEALTH STAGES (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING COMPANY] | 1 | |
| sorbitol | INACTIVE INGREDIENT | 506T60A25R | CREST PRO-HEALTH STAGES (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING COMPANY] | 1 | |
| water | INACTIVE INGREDIENT | 059QF0KO0R | CREST PRO-HEALTH STAGES (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING COMPANY] | 1 | |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37000-673-04 | 37000067304 | 120 g in 1 TUBE (37000-673-04) | 120 g | 2008-08-01 | 2021-12-01 | No | No | Current |