Fortinia ID

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Fortinia ID
Generic name: PHENOL
Manufacturer: The Podiatree Company
Product type: HUMAN OTC DRUG
SPL set ID: 60c88eb7-22fe-4881-e053-2a91aa0a70ce
SPL ID: 47e36787-66d5-d17e-e063-6394a90a0d73
Version: 3
Effective date: 2026-01-08
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:26:53

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Fortinia ID	openfda.brand_name
generic name		PHENOL	openfda.generic_name
manufacturer name		The Podiatree Company	openfda.manufacturer_name
ndc	package	54633-216-15	openfda.package_ndc
ndc	product	54633-216	openfda.product_ndc
ndc11	package	54633021615	derived:openfda.package_ndc
rxcui		199858	openfda.rxcui
spl id		47e36787-66d5-d17e-e063-6394a90a0d73	id
spl set id		60c88eb7-22fe-4881-e053-2a91aa0a70ce	set_id
unii		339NCG44TV	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

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

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.