Summit E2 Foaming E2
- Product NDC
- 79532-021
- 11-digit product format
- 795320021
- Labeler code
- 79532
- Product ID
- 79532-021_ed364ad8-d5eb-4366-e053-2995a90a2714
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium chloride 0.13%
- Dosage form
- SOAP
- Route
- TOPICAL
- Labeler
- Dyno Manufacturing
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-11-01
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 g/850mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 79532-021-85 | 79532002185 | 850 mL in 1 BOTTLE (79532-021-85) | 850 ml | 2022-11-01 | 0000-00-00 | No | No | Current |