NDC 52261-0703 - Forticept Green Butter Antimicrobial Gel
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 52261-0703
- Package NDCs from labels
- 52261-0703-0, 52261-0703-1
- Manufacturer
- Cosco International, Inc.
- Effective date
- 2016-11-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Forticept Green Butter Antimicrobial Gel - Cosco International, Inc. | Cosco International, Inc. | 2016-11-30 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52261-0703-0 | Forticept Green Butter Antimicrobial Gel | 150 g in 1 CAN | Gel | 150 | 1 | |
| 52261-0703-1 | Forticept Green Butter Antimicrobial Gel | 240 g in 1 CAN | Gel | 240 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 52261-0703 | FORTICEPT GREEN BUTTER ANTIMICROBIAL GEL (BENZETHONIUM CHLORIDE) GEL [COSCO INTERNATIONAL, INC.] | 1 | 2 package rows | 20161201_ef7846ce-7fc7-4b1e-8d62-cda572ee2418.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 |
|---|---|---|---|---|---|---|
| CPAP Mask cleaning wipes | BENZETHONIUM CHLORIDE AND BENZALKONIUM CHLORIDE | JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD. | 412e6fec-5af5-45f7-8c6b-393b884e161c | 2019-06-07 | Warnings | PH41D05744 |
| Hand Wipes | CHLORHEXIDINE DIGLUCONATE AND BENZETHONIUM CHLORIDE | JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD. | 181e5fa0-ddda-4783-a0b5-ff95bfce6b36 | 2017-10-09 | Warnings | PH41D05744 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.