Benzalkonium chloride
- Product NDC
- 75712-575
- 11-digit product format
- 757120575
- Labeler code
- 75712
- Product ID
- 75712-575_4c0faf92-e9ab-2047-e063-6394a90a3f9a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Old East Main Co.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-21
- 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 | 1046593 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75712-575-96 | Benzalkonium chloride | 221 mL in 1 BOTTLE, PLASTIC | LIQUID | 221 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 75712-575-96 | 75712057596 | 221 mL in 1 BOTTLE, PLASTIC (75712-575-96) | 221 ml | 2026-01-21 | No | No | Current |