PreviDent
- Product NDC
- 0126-0075
- 11-digit product format
- 001260075
- Labeler code
- 0126
- Product ID
- 0126-0075_33c288df-0d48-404b-b280-88ff8ea4a7fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- Colgate-Palmolive Company
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2009-07-06
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 13 mg/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record