Kevo-Prophen

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: Kevo-Prophen
Generic name: JUNIPER TAR
Manufacturer: Faeve, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 4fe773a8-77cd-831e-e063-6294a90ae2ca
SPL ID: 4fe773a8-77ce-831e-e063-6294a90ae2ca
Version: 1
Effective date: 2026-04-20
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:35:57

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Kevo-Prophen	openfda.brand_name
generic name		JUNIPER TAR	openfda.generic_name
manufacturer name		Faeve, LLC	openfda.manufacturer_name
ndc	package	87607-001-01	openfda.package_ndc
ndc	product	87607-001	openfda.product_ndc
ndc11	package	87607000101	derived:openfda.package_ndc
spl id		4fe773a8-77ce-831e-e063-6294a90ae2ca	id
spl set id		4fe773a8-77cd-831e-e063-6294a90ae2ca	set_id
unii		1Q84T0P2G3	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 Use only as directed Read and follow directions on label Avoid contact with eyes and muscous membranes. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician. If pregnant or breast feeding, ask a physician before use. Keep out of reach of children If swallowed, get medical help or contact Poison Control Center right away. DO NOT USE on puncture wounds on cut, irritated, or open skin.

Reported adverse events (FAERS/openFDA)#

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