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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 16902YVY2B | PODOPHYLLUM RESIN | 9000-55-9 | PODOPHYLLUM RESIN |
Packages
| 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 | Historical |