Foaming Antibacterial Hand
- Product NDC
- 67502-110
- 11-digit product format
- 675020110
- Labeler code
- 67502
- Product ID
- 67502-110_5dcf421a-3c2a-1477-e063-6394a90a0eab
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Intercon Chemical Company
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-06-29
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 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
- Foaming Antibacterial Hand
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 1 mg/mL |
Harmonized UNII identifiers#
UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table| Identifier | FDA.report destination |
|---|
| F5UM2KM3W7 | Internal UNII lookup |
Harmonized RxCUI identifiers#
RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table| Identifier | FDA.report destination |
|---|
| 1233282 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
SPL set identifiers page 1 of 1 · 1 matching rows.
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67502-110-08 | 67502011008 | 1000 mL in 1 BOTTLE, PUMP (67502-110-08) | 1000 ml | 2026-10-14 | No | No | Current |
| 67502-110-85 | 67502011085 | 850 mL in 1 BOTTLE, PUMP (67502-110-85) | 850 ml | 2026-06-29 | No | No | Current |