Podocon 25
- Product NDC
- 72162-1117
- 11-digit product format
- 721621117
- Labeler code
- 72162
- Product ID
- 72162-1117_76554f72-0e40-4ea9-a24e-8ab8c726c371
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Podophyllum resin
- Dosage form
- TINCTURE
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- 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 |
|---|
| 72162-1117-2 | Podocon 25 | 1 in 1 CARTON | TINCTURE | 1 | | 100 |
| 72162-1117-2 | Podocon 25 | 15 mL in 1 BOTTLE, WITH APPLICATOR | TINCTURE | 15 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1117 | PODOCON 25 (PODOPHYLLUM RESIN) TINCTURE [BRYANT RANCH PREPACK] | 100 | Current NDC, 2 package rows | 20241228_4e1e23c5-9d08-4ff5-99f2-f8c0aa619035.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1117-2 | 72162111702 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (72162-1117-2) / 15 mL in 1 BOTTLE, WITH APPLICATOR | 2024-12-24 | No | No | Historical |