TERPENICOL

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: TERPENICOL
Generic name: UNDECYLENIC ACID
Manufacturer: Blaine Labs Inc.
Product type: HUMAN OTC DRUG
SPL set ID: efd99ed1-07d3-4862-ae47-883f7d1c91c6
SPL ID: f6a16024-2fa1-44ff-a718-af2dc7ae822e
Version: 3
Effective date: 2023-12-21
Source export date: 2026-11-06
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:23:11

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		M005	openfda.application_number
brand name		TERPENICOL	openfda.brand_name
generic name		UNDECYLENIC ACID	openfda.generic_name
manufacturer name		Blaine Labs Inc.	openfda.manufacturer_name
ndc	package	63347-601-01	openfda.package_ndc
ndc	product	63347-601	openfda.product_ndc
ndc11	package	63347060101	derived:openfda.package_ndc
spl id		f6a16024-2fa1-44ff-a718-af2dc7ae822e	id
spl set id		efd99ed1-07d3-4862-ae47-883f7d1c91c6	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

WARNINGS: 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 NOT 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.

Reported adverse events (FAERS/openFDA)#

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