Antibiotic Free Wound Gel and Pain Relief
- Product NDC
- 51142-352
- 11-digit product format
- 511420352
- Labeler code
- 51142
- Product ID
- 51142-352_cb93e793-fe4e-452c-e053-2995a90a7333
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride and Lidocaine Hydrochloride
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- ASO LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-03-21
- Marketing end
- 2022-09-01
- Substance
- LIDOCAINE HYDROCHLORIDE; BENZALKONIUM CHLORIDE
- Active strength
- 2 g/100mL; 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 51142-352-14 | 51142035214 | 1 TUBE in 1 CARTON (51142-352-14) > 14 mL in 1 TUBE | 1 tube | 2019-10-18 | 0000-00-00 | No | No | Current |
| 51142-352-32 | 51142035232 | 1 TUBE in 1 CARTON (51142-352-32) > 28 mL in 1 TUBE | 1 tube | 2017-03-21 | 0000-00-00 | No | No | Current |