NUPRO 60 Second Fluoride Foam
- Product NDC
- 65222-113
- 11-digit product format
- 652220113
- Labeler code
- 65222
- Product ID
- 65222-113_dc22f86a-7d06-47f7-8506-1c5124b89389
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- AEROSOL, FOAM
- Route
- DENTAL
- Labeler
- Dentsply Professional
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1997-04-01
- Marketing end
- 2022-12-28
- Substance
- SODIUM FLUORIDE
- Active strength
- 27 mg/g
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65222-113-44 | 65222011344 | 1 CAN in 1 CARTON (65222-113-44) > 125 g in 1 CAN | 1 can | 1997-04-01 | 0000-00-00 | No | No | Current |