Podocon 25
- Product NDC
- 71335-2925
- 11-digit product format
- 713352925
- Labeler code
- 71335
- Product ID
- 71335-2925_c4e909ba-10b5-4c09-afea-4c5d151f657a
- 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 |
|---|
| 71335-2925-1 | Podocon 25 | 15 mL in 1 BOTTLE, WITH APPLICATOR | TINCTURE | 15 | | 100 |
| 71335-2925-1 | Podocon 25 | 1 in 1 CARTON | TINCTURE | 1 | | 100 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2925-1 | 71335292501 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (71335-2925-1) / 15 mL in 1 BOTTLE, WITH APPLICATOR | 2025-10-21 | No | No | Current |