Pro Plus
- Product NDC
- 80069-002
- 11-digit product format
- 800690002
- Labeler code
- 80069
- Product ID
- 80069-002_963940ae-9d46-4bce-8198-268c800c9294
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine HCl, Tetracaine HCl
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Dermal Source, Inc.
- Application
- part346
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2006-03-03
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE; TETRACAINE HYDROCHLORIDE
- Active strength
- 40 mg/29.5735mL; mg/29.5735mL
- 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 |
|---|
| 80069-002-01 | 80069000201 | 25.8768 mL in 1 BOTTLE, PLASTIC (80069-002-01) | 25.8768 ml | 2006-03-03 | 0000-00-00 | No | No | Current |