Unguentine

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: Unguentine
Generic name: PHENOL, ZINC OXIDE
Manufacturer: Oakhurst Company
Product type: HUMAN OTC DRUG
SPL set ID: 327038a1-b825-1199-e063-6394a90a7f5f
SPL ID: 327038a1-b826-1199-e063-6394a90a7f5f
Version: 1
Effective date: 2025-04-10
Source export date: 2026-10-12
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:30:50

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		Unguentine	openfda.brand_name
generic name		PHENOL, ZINC OXIDE	openfda.generic_name
manufacturer name		Oakhurst Company	openfda.manufacturer_name
ndc	package	45728-446-99	openfda.package_ndc
ndc	product	45728-446	openfda.product_ndc
ndc11	package	45728044699	derived:openfda.package_ndc
spl id		327038a1-b826-1199-e063-6394a90a7f5f	id
spl set id		327038a1-b825-1199-e063-6394a90a7f5f	set_id
unii		339NCG44TV	openfda.unii
unii		SOI2LOH54Z	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 Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns When using this product Do not get into eyes Do not apply to large areas of body Do not bandage Do not exceed recommended dosage Stop use and ask a docter if the condition persists or gets worse the condition does not improve within 7 days Keep out of reach of children In case of accidental ingestion, seel professional assistance or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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