Benzalkonium chloride
- Product NDC
- 11673-681
- 11-digit product format
- 116730681
- Labeler code
- 11673
- Product ID
- 11673-681_4b1fc280-f1ee-ce33-e063-6294a90a4a96
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- First Aid Antiseptic Foam
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Target Corporation
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-11
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1.3 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
- Benzalkonium chloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 1.3 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 1020365 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11673-681-23 | Benzalkonium chloride | 68 mL in 1 BOTTLE, PUMP | AEROSOL, FOAM | 68 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 11673-681-23 | 11673068123 | 68 mL in 1 BOTTLE, PUMP (11673-681-23) | 68 ml | 2025-12-11 | No | No | Historical |