UltraCare
- Product NDC
- 51206-201
- 11-digit product format
- 512060201
- Labeler code
- 51206
- Product ID
- 51206-201_ef1abc86-26ba-48a2-b40f-a2f4a5291545
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine
- Dosage form
- GEL
- Route
- DENTAL
- Labeler
- Ultradent Products, Inc.
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 1986-06-01
- Marketing end
- 2024-08-31
- Substance
- BENZOCAINE
- Active strength
- 200 mg/mL
- 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 |
|---|
| 51206-201-01 | 51206020101 | 30 mL in 1 BOTTLE (51206-201-01) | 30 ml | 1986-06-01 | 2022-06-18 | No | No | Current |
| 51206-201-02 | 51206020102 | 1 SYRINGE, PLASTIC in 1 BOX (51206-201-02) > 30 mL in 1 SYRINGE, PLASTIC | | 1986-06-01 | 2023-08-31 | No | No | Current |