Benzethonium Chloride and Dyclonine Hydrochloride
- Product NDC
- 11822-0779
- 11-digit product format
- 118220779
- Labeler code
- 11822
- Product ID
- 11822-0779_c792fa8a-66e6-2b8b-e053-2995a90a6088
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Liquid Bandage
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Rite Aid Corporation
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-02-01
- Marketing end
- 0000-00-00
- Substance
- BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
- Active strength
- 0 mg/30mL; mg/30mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-0779 | BENZETHONIUM CHLORIDE AND DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [RITE AID CORPORATION] | 4 | Legacy NDC | 20241213_ae42b754-9a06-6e80-e053-2a95a90a740d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0779-3 | 11822077903 | 30 mL in 1 BOTTLE, WITH APPLICATOR (11822-0779-3) | 30 ml | 2020-02-01 | 0000-00-00 | No | No | Current |