Summit 367 Antibacterial Foam
- Product NDC
- 23590-200
- 11-digit product format
- 235900200
- Labeler code
- 23590
- Product ID
- 23590-200_509f01c4-79a0-69d4-e063-6394a90a4a83
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- R.L. Williams Company
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-04-29
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Summit 367 Antibacterial Foam
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 1233282 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 23590-200-10 | Summit 367 Antibacterial Foam | 850 mL in 1 BOTTLE, PUMP | SOLUTION | 850 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 23590-200-10 | 23590020010 | 850 mL in 1 BOTTLE, PUMP (23590-200-10) | 850 ml | 2026-04-29 | No | No | Historical |