Benzalkonium chloride
- Product NDC
- 83986-912
- 11-digit product format
- 839860912
- Labeler code
- 83986
- Product ID
- 83986-912_5a98e396-868f-47b9-e063-6294a90a9d41
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium chloride
- Dosage form
- SWAB
- Route
- TOPICAL
- Labeler
- UpLift Brands, LLC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-03
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .13 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
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 | .13 mg/mL |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83986-912-20 | 83986091220 | 53 mL in 1 CELLO PACK (83986-912-20) | 53 ml | 2026-09-03 | No | No | Current |
| 83986-912-90 | 83986091290 | 261 mL in 1 CELLO PACK (83986-912-90) | 261 ml | 2026-09-03 | No | No | Current |