Tripenicol C

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: Tripenicol C
Generic name: UNDECYLENIC ACID
Manufacturer: Trifluent Pharma LLC
Product type: HUMAN OTC DRUG
SPL set ID: 0a7477da-370f-451f-8993-8c675c168696
SPL ID: c872059f-48b3-479c-8c1c-0893d67cc1e2
Version: 4
Effective date: 2025-10-14
Source export date: 2026-10-12
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:31:43

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M005	openfda.application_number
brand name		Tripenicol C	openfda.brand_name
generic name		UNDECYLENIC ACID	openfda.generic_name
manufacturer name		Trifluent Pharma LLC	openfda.manufacturer_name
ndc	package	73352-555-01	openfda.package_ndc
ndc	product	73352-555	openfda.product_ndc
ndc11	package	73352055501	derived:openfda.package_ndc
rxcui		1250978	openfda.rxcui
rxcui		2677085	openfda.rxcui
spl id		c872059f-48b3-479c-8c1c-0893d67cc1e2	id
spl set id		0a7477da-370f-451f-8993-8c675c168696	set_id
unii		K3D86KJ24N	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

WARNING Do not use on children under two years of age unless directed by a physician. For external use only. Avoid contact with eyes. If irritation occurs or if there is no improvement within four (4) weeks (for Athlete's Foot or Ringworm) or within two (2) weeks (for Jock Itch), discontinue use and consult a physician. Keep this and all drugs out of reach of children. In case of accidental ingestion, seek professional assistance or contact poison control center immediately (800)-222-1222.

Reported adverse events (FAERS/openFDA)#

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