Benzethonium chloride Plus Dyclonine hydrochloride
- Product NDC
- 11673-629
- 11-digit product format
- 116730629
- Labeler code
- 11673
- Product ID
- 11673-629_c7b5e90e-f024-1691-e053-2995a90a89f6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Liquid Bandage
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Target Corporation
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-12-01
- Marketing end
- 0000-00-00
- Substance
- BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
- Active strength
- 0 mg/10mL; mg/10mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-629 | BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [TARGET CORPORATION] | 7 | Legacy NDC | 20241213_dfb69610-b2a8-4420-b41e-2f3e1744433e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-629-10 | 11673062910 | 10 mL in 1 BOTTLE, WITH APPLICATOR (11673-629-10) | 10 ml | 2017-12-01 | 0000-00-00 | No | No | Current |