Forticept Antimicrobial Gel
- Product NDC
- 52261-0701
- 11-digit product format
- 522610701
- Labeler code
- 52261
- Product ID
- 52261-0701_93d1511d-c343-47be-8261-2632b4dd8dcb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzethonium Chloride
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Cosco International, Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-10-27
- Marketing end
- 0000-00-00
- Substance
- BENZETHONIUM CHLORIDE; THYMOL
- Active strength
- 1 g/1000g; g/1000g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52261-0701-0 | Forticept Antimicrobial Gel | 60 g in 1 TUBE | Gel | 60 | | 2 |
| 52261-0701-1 | Forticept Antimicrobial Gel | 90 g in 1 TUBE | Gel | 90 | | 2 |
| 52261-0701-2 | Forticept Antimicrobial Gel | 120 g in 1 TUBE | Gel | 120 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52261-0701 | FORTICEPT ANTIMICROBIAL GEL (BENZETHONIUM CHLORIDE) GEL [COSCO INTERNATIONAL, INC.] | 2 | Legacy NDC, 3 package rows | 20161028_9da1bd69-eab6-493b-8f5c-5247f8af237c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 52261-0701-0 | 52261070100 | 60 g in 1 TUBE | 60 g | Historical |
| 52261-0701-1 | 52261070101 | 90 g in 1 TUBE | 90 g | Historical |
| 52261-0701-2 | 52261070102 | 120 g in 1 TUBE | 120 g | Historical |