ANTIBACTERIAL HANDWASH
- Product NDC
- 76176-041
- 11-digit product format
- 761760041
- Labeler code
- 76176
- Product ID
- 76176-041_5c2342b4-9237-b0ab-e063-6294a90a0f5a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- antibacterial hand soap benzalkonium chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Ningbo Liyuan Daily Chemical Products Co.,Ltd.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-08-01
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .13 g/100mL
- 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
- ANTIBACTERIAL HANDWASH
- Brand name suffix
- PEACH DREAM
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | .13 g/100mL |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76176-041-01 | 76176004101 | 400 mL in 1 BOTTLE (76176-041-01) | 400 ml | 2018-08-01 | 0000-00-00 | No | No | Current |