Benzethonium chloride Plus Dyclonine hydrochloride
- Product NDC
- 72446-100
- 11-digit product format
- 724460100
- Labeler code
- 72446
- Product ID
- 72446-100_42789589-4116-8081-e063-6294a90af33c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Liquid Bandage
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Hudson Health LLC
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-09-01
- Substance
- BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
- Active strength
- 2; 7.5 mg/mL; mg/mL
- 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/mL |
| DYCLONINE HYDROCHLORIDE | 7.5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | PH41D05744, ZEC193879Q |
| Rxcui | 1048366 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72446-100-01 | Benzethonium chloride Plus Dyclonine hydrochloride | 29.6 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 29.6 | | 1 |
| 72446-100-01 | Benzethonium chloride Plus Dyclonine hydrochloride | 1 in 1 CARTON | LIQUID | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72446-100-01 | 72446010001 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (72446-100-01) / 29.6 mL in 1 BOTTLE, WITH APPLICATOR | 2018-09-01 | No | No | Historical |