Premier Solutions Liquid Bandage
- Product NDC
- 56104-246
- 11-digit product format
- 561040246
- Labeler code
- 56104
- Product ID
- 56104-246_4096871d-bc42-b86a-e063-6294a90afe8b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzethonium chloride Dyclonine hydrochloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Premier Brands of America, Inc.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-06-16
- Substance
- BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
- Active strength
- .2; .75 mg/10mL; mg/10mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Premier Solutions Liquid Bandage
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BENZETHONIUM CHLORIDE | .2 mg/10mL |
| DYCLONINE HYDROCHLORIDE | .75 mg/10mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| PH41D05744 | Internal UNII lookup |
| ZEC193879Q | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| e196d4c2-a93e-a03c-e053-2995a90a3ea3 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 1da7d10e-498b-41dd-970f-0f5bd7432f39 | Product name | 1 | 20190228 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 56104-246-01 | Premier Solutions Liquid Bandage | 10 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 10 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 56104-246 | PREMIER SOLUTIONS LIQUID BANDAGE (BENZETHONIUM CHLORIDE DYCLONINE HYDROCHLORIDE) LIQUID [PREMIER BRANDS OF AMERICA, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241016_e196d4c2-a93e-a03c-e053-2995a90a3ea3.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Povidone-Iodine Pad | POVIDONE-IODINE | Shandong Haiyan Medical Manufacture Co., Ltd. | c9187a07-92d5-15ac-e053-2995a90af4cb | 2022-03-19 | Warnings | M003 |
| Alcohol Prep Pad | ISOPROPYL ALCOHOL | Shandong Haiyan Medical Manufacture Co., Ltd. | 1a117840-22d0-4a88-b1a6-e43162a444ab | 2022-03-19 | Warnings | M003 |
| FIRSTAR BZK Antiseptic Towelette | BENZALKONIUM CHLORIDE | JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD. | 28591a97-9291-48c8-a8e3-c419180331b3 | 2021-07-06 | Warnings | M003 |
| Bactine Max | BENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDE | WellSpring Pharmaceutical Corporation | 28e8a311-20a4-45a1-8d5d-ca42b101c275 | 2021-02-24 | Warnings | M003 |
| Hand Sanitizer Lemon 2oz | ALCOHOL | Ningbo Rejoice International | b0a4159a-cb07-4ce6-e053-2995a90a76e7 | 2020-10-02 | Warnings | M003 |
| Sanix Alcohol Hand Rub | ALCOHOL | Topiderm, Inc | a4fbb714-4f20-400a-ab98-f1c8807ce6fc | 2020-03-24 | Warnings | M003 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 56104-246-01 | 56104024601 | 10 mL in 1 BOTTLE, WITH APPLICATOR (56104-246-01) | 10 ml | 2022-06-16 | 0000-00-00 | No | No | Current |