FORTINIA ID- phenol liquid 
The Podiatree Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active Ingredient

Phenol 1.5%

Purpose

First Aid Antiseptic

Uses

Warnings

For external use only

Do not use

  • in eyes
  • with bandages
  • on large areas of the body
  • longer than one week unless directed by a doctor
  • stop use and consult a doctor if condition persists
  • in case of deep puncture wounds, animal bites, or serious burns, consult a doctor
  • if known to be sensitive to any ingredients in this product

Stop use and ask a doctor or pharmacist if skin irritation or sensitivity develops or increases or if the condition persists or gets worse.

When using this product

  • Check skin for sensitivity to phenol prior to application
  • Use caution when applying as this product will stain skin and clothing

KEEP OUT OF REACH OF CHILDREN

Directions

Other Information

Store at controlled room temperature

Inactive Ingredients

Acetone, resorcinol, SD alcohol (13%), water

Questions or Suggestions?

1.855.763.8733 or visit us at www.thepodiatreecompany.com. Our commitment to you is 100% satisfaction. If you are not

completely satisfied, please contact us directly for a full refund.

PRINCIPAL DISPLAY PANEL

label

FORTINIA ID 
phenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54633-216
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PHENOL (UNII: 339NCG44TV) (PHENOL - UNII:339NCG44TV) PHENOL1.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ACETONE (UNII: 1364PS73AF)  
RESORCINOL (UNII: YUL4LO94HK)  
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54633-216-1514.8 mL in 1 BOTTLE; Type 0: Not a Combination Product01/03/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/03/2017
Labeler - The Podiatree Company (078656000)

Revised: 12/2017
Document Id: 60c88eb7-22ff-4881-e053-2a91aa0a70ce
Set id: 60c88eb7-22fe-4881-e053-2a91aa0a70ce
Version: 2
Effective Time: 20171220
 
The Podiatree Company