Benzethonium chloride Plus Dyclonine hydrochloride
- Product NDC
- 50804-755
- 11-digit product format
- 508040755
- Labeler code
- 50804
- Product ID
- 50804-755_c6b155d7-004f-c1d3-e053-2995a90abc8f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Liquid Bandage
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Geiss Destin & Dunn Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-07-09
- Marketing end
- 0000-00-00
- Substance
- BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
- Active strength
- 0 mg/9mL; mg/9mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50804-755-03 | 50804075503 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (50804-755-03) > 9 mL in 1 BOTTLE, WITH APPLICATOR | 2021-07-09 | 0000-00-00 | No | No | Current |