Benzethonium chloride Plus Dyclonine hydrochloride
- Product NDC
- 37808-512
- 11-digit product format
- 378080512
- Labeler code
- 37808
- Product ID
- 37808-512_4094cbfe-fb3e-0d58-e063-6394a90a47cc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Liquid Bandage
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- HEB
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-12-22
- Substance
- BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
- Active strength
- .2; .75 mg/9mL; mg/9mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Benzethonium chloride Plus Dyclonine hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZETHONIUM CHLORIDE | .2 mg/9mL |
| DYCLONINE HYDROCHLORIDE | .75 mg/9mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | PH41D05744, ZEC193879Q |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37808-512-03 | Benzethonium chloride Plus Dyclonine hydrochloride | 9 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 9 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-512 | BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [HEB] | 7 | Current NDC, Legacy NDC, 1 package rows | 20241213_40b71196-a2ac-4a44-8046-c448d066baa2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-512-03 | 37808051203 | 9 mL in 1 BOTTLE, WITH APPLICATOR (37808-512-03) | 9 ml | 2017-12-22 | 0000-00-00 | No | No | Current |