Antibiotic Free Wound Gel
- Product NDC
- 51142-650
- 11-digit product format
- 511420650
- Labeler code
- 51142
- Product ID
- 51142-650_ba4c3694-1b15-0c13-e053-2995a90af6d5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- ASO LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-03-21
- Marketing end
- 2022-11-12
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51142-650-32 | 51142065032 | 1 TUBE in 1 CARTON (51142-650-32) > 28 mL in 1 TUBE | 1 tube | 2017-03-21 | 2022-11-12 | No | No | Current |