Polident
- Product NDC
- 0135-0711
- 11-digit product format
- 001350711
- Labeler code
- 0135
- Product ID
- 0135-0711_4c01ca1f-f991-491d-bfb8-61ad548373ea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- sodium fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-01-04
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 0135-0711-01 | 00135071101 | 500 mL in 1 BOTTLE (0135-0711-01) | 500 ml | 2021-01-04 | 0000-00-00 | No | No | Current |
| 0135-0711-02 | 00135071102 | 333 mL in 1 BOTTLE (0135-0711-02) | 333 ml | 2021-01-04 | 0000-00-00 | No | No | Current |
| 0135-0711-03 | 00135071103 | 59 mL in 1 BOTTLE (0135-0711-03) | 59 ml | 2021-01-04 | 0000-00-00 | No | No | Current |