BENZALKONIUM CHLORIDE
- Product NDC
- 33992-8991
- 11-digit product format
- 339928991
- Labeler code
- 33992
- Product ID
- 33992-8991_b6fdf78f-4b9a-aca7-e053-2995a90a991c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Greenbrier International, Inc.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-08-25
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/g
- 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 |
|---|
| 33992-8991-1 | 33992899101 | 369 g in 1 BOTTLE (33992-8991-1) | 369 g | 2020-08-25 | 0000-00-00 | No | No | Current |