Benzethonium chloride Plus Dyclonine hydrochloride
- Product NDC
- 56104-040
- 11-digit product format
- 561040040
- Labeler code
- 56104
- Product ID
- 56104-040_c74064c0-0e8a-4a5c-e053-2a95a90a1e86
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Liquid Bandage
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Premier Brands of America Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-01-03
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 56104-040-03 | 56104004003 | 9 mL in 1 BOTTLE, WITH APPLICATOR (56104-040-03) | 9 ml | 2018-01-03 | 0000-00-00 | No | No | Current |
| 56104-040-30 | 56104004030 | 30 mL in 1 BOTTLE (56104-040-30) | 30 ml | 2018-01-03 | 0000-00-00 | No | No | Current |