Liquid Bandage
- Product NDC
- 56104-502
- 11-digit product format
- 561040502
- Labeler code
- 56104
- Product ID
- 56104-502_4094375b-31ea-3c3a-e063-6294a90ad8f6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzethonium chloride Plus Dyclonine hydrochloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Premier Brands of America Inc.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-09-11
- 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
- Liquid Bandage
- 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 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 56104-502-00 | Liquid Bandage | 29.6 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 29.6 | | 5 |
| 56104-502-00 | Liquid Bandage | 1 in 1 CARTON | LIQUID | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 56104-502 | LIQUID BANDAGE (BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE) LIQUID [PREMIER BRANDS OF AMERICA INC.] | 4 | Current NDC, 2 package rows | 20241016_051b68f9-5d6c-3cd7-e063-6394a90aeb35.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 56104-502-00 | 56104050200 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (56104-502-00) / 29.6 mL in 1 BOTTLE, WITH APPLICATOR | 2023-09-11 | No | No | Current |