CICLOPIROX 3%
- Product NDC
- 72934-1042
- 11-digit product format
- 729341042
- Labeler code
- 72934
- Product ID
- 72934-1042_89574010-4281-0d72-e053-2995a90a5295
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CICLOPIROX 3%
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Sincerus Florida, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-05-20
- Marketing end
- 0000-00-00
- Substance
- CICLOPIROX OLAMINE
- Active strength
- 3 g/100g
- Pharmacologic classes
- Decreased DNA Replication [PE],Decreased Protein Synthesis [PE],Decreased RNA Replication [PE],Protein Synthesis Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72934-1042-2 | CICLOPIROX 3% | 30 g in 1 BOTTLE, PUMP | GEL | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72934-1042 | CICLOPIROX 3% GEL [SINCERUS FLORIDA, LLC] | 1 | Legacy NDC, 1 package rows | 20190521_89574010-4280-0d72-e053-2995a90a5295.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 72934-1042-2 | 72934104202 | 30 g in 1 BOTTLE, PUMP | 30 g | Historical |