Colgate Hydris Dry Mouth
- Product NDC
- 35000-210
- 11-digit product format
- 350000210
- Labeler code
- 35000
- Product ID
- 35000-210_52a8441f-c61b-4021-96e9-a5e333b9bb10
- 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
- 2017-12-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 2 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 35000-210-71 | 35000021071 | 1 TUBE in 1 CARTON (35000-210-71) > 119 g in 1 TUBE | 1 tube | 2017-12-01 | 2022-01-01 | No | No | Current |