PROTOXIN
- Product NDC
- 71066-0001
- 11-digit product format
- 710660001
- Labeler code
- 71066
- Product ID
- 71066-0001_41280d2a-9232-5800-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Clostridium botulinum Toxin Type A
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- PROTOX Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2016-11-10
- Marketing end
- 0000-00-00
- Substance
- CLOSTRIDIUM BOTULINUM
- Active strength
- 10 g/10mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 71066-0001-1 | PROTOXIN | 10 mL in 1 VIAL | GEL | 10 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71066-0001 | PROTOXIN (CLOSTRIDIUM BOTULINUM TOXIN TYPE A) GEL [PROTOX INC.] | 1 | Legacy NDC, 1 package rows | 20161114_41280d2a-9231-5800-e054-00144ff88e88.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 71066-0001-1 | 71066000101 | 10 mL in 1 VIAL | 10 ml | Historical |