MedPath

Podophyllin

Generic Name
Podophyllin
Brand Names
Cantharone Plus
Drug Type
Small Molecule
Chemical Formula
C88H92O34
CAS Number
9000-55-9
Unique Ingredient Identifier
16902YVY2B

Overview

Podophyllin is a resin extracted from the roots of Podophyllum peltatum (American mandrake) and Podophyllum emodi, which contains numerous compounds, amongst which is podophyllin (as well as the drug podophyllotoxin). Podophyllin is the principal active component. Podophyllin arrests mitosis in metaphase.

Indication

25% podophyllin (in benzoin tincture) is indicated for the removal of soft genital (venereal) warts (condylomata acuminata).

Associated Conditions

  • Soft genital warts

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Bryant Ranch Prepack
63629-8699
TOPICAL
1 mg in 4 mL
2/23/2022
Sincerus Florida, LLC
72934-9036
TOPICAL
5 g in 100 g
5/17/2019
Padagis US LLC
0574-0601
TOPICAL
1 mg in 4 mL
11/15/2018

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
WART-OFF PAINT bottle
18915
Pharmacare Laboratories Pty Ltd
Medicine
A
9/30/1991

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
VERBAN ONT
welcker-lyster ltd., division of technilab inc.
00206342
Ointment - Topical
2 G / 100 G
12/31/1963
CANTHARONE PLUS
dormer laboratories inc.
00772011
Liquid - Topical
2 %
12/31/1984
CANTHACUR-PS
paladin pharma inc.
00589500
Liquid - Topical
5 %
12/31/1983
PODOFILM LIQ 250MG/ML
paladin pharma inc.
00598208
Liquid - Topical
250 MG / ML
12/31/1984

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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