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
IngredientStrength
PODOPHYLLUM RESIN1 mg/4mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
16902YVY2BInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
de96dc6e-e6d1-4383-9ce1-4d06bac08e00Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0574-0601-15Podocon 251 in 1 CARTONTINCTURE14
0574-0601-15Podocon 2515 mL in 1 BOTTLE, WITH APPLICATORTINCTURE154

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0574-0601-15ML - Milliliter0574-0601101cce12-461e-4120-b8c0-d6533f27580412014-10-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PODOPHYLLUM RESINACTIVE INGREDIENT16902YVY2BPODOCON 25 (PODOPHYLLUM RESIN) TINCTURE [PADDOCK LABORATORIES, LLC]1
PODOPHYLLUM RESINACTIVE MOIETY16902YVY2BPODOCON 25 (PODOPHYLLUM RESIN) TINCTURE [PADDOCK LABORATORIES, LLC]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MPODOCON 25 (PODOPHYLLUM RESIN) TINCTURE [PADDOCK LABORATORIES, LLC]1
STYRAX BENZOIN RESININACTIVE INGREDIENTFE663Z8IROPODOCON 25 (PODOPHYLLUM RESIN) TINCTURE [PADDOCK LABORATORIES, LLC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0574-0601PODOCON 25 (PODOPHYLLUM RESIN) TINCTURE [PADAGIS US LLC]4Current NDC, Legacy NDC, 2 package rows20241208_de96dc6e-e6d1-4383-9ce1-4d06bac08e00.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Podocon 25PODOPHYLLUM RESINPadagis US LLCde96dc6e-e6d1-4383-9ce1-4d06bac08e002022-06-30Warnings, Adverse reactionsExact identifier
ndc (product): 0574-0601

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0574-0601-15005740601151 BOTTLE, WITH APPLICATOR in 1 CARTON (0574-0601-15) / 15 mL in 1 BOTTLE, WITH APPLICATOR1990-09-010000-00-00NoNoCurrent