Podocon 25
- Product NDC
- 0574-0601
- 11-digit product format
- 005740601
- Labeler code
- 0574
- Product ID
- 0574-0601_e2ac9612-bded-4eea-a664-f941416583fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Podophyllum resin
- Dosage form
- TINCTURE
- Route
- TOPICAL
- Labeler
- Padagis US LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1990-09-01
- Substance
- PODOPHYLLUM RESIN
- Active strength
- 1 mg/4mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Podocon 25
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PODOPHYLLUM RESIN | 1 mg/4mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 16902YVY2B |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0574-0601-15 | Podocon 25 | 1 in 1 CARTON | TINCTURE | 1 | | 4 |
| 0574-0601-15 | Podocon 25 | 15 mL in 1 BOTTLE, WITH APPLICATOR | TINCTURE | 15 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0574-0601 | PODOCON 25 (PODOPHYLLUM RESIN) TINCTURE [PADAGIS US LLC] | 4 | Current NDC, Legacy NDC, 2 package rows | 20241208_de96dc6e-e6d1-4383-9ce1-4d06bac08e00.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0574-0601-15 | 00574060115 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0574-0601-15) / 15 mL in 1 BOTTLE, WITH APPLICATOR | 1990-09-01 | 0000-00-00 | No | No | Current |