COLGATE
- Product NDC
- 35000-908
- Requested package NDC
- 35000-908-81
- 11-digit product format
- 350000908
- Labeler code
- 35000
- Product ID
- 35000-908_330b28ce-dd8b-4370-a245-6c3a515226b2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- Colgate-Palmolive Company
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2011-07-26
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 1 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 35000-908-81 | COLGATEMAX WHITE WITH MINI BRIGHT STRIPS Crystal MINT | 130 g in 1 BOTTLE | GEL, DENTIFRICE | 130 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 35000-908 | COLGATE MAX WHITE WITH MINI BRIGHT STRIPS CRYSTAL MINT (SODIUM FLUORIDE) GEL, DENTIFRICE [COLGATE-PALMOLIVE COMPANY] | 2 | Legacy NDC, 1 package rows | 20241020_74df027f-c3cb-40e7-89b1-5973d14d27b4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35000-908-81 | 35000090881 | 130 g in 1 BOTTLE (35000-908-81) | 130 g | 2011-07-26 | 0000-00-00 | No | No | Current |