END-ZIT

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: END-ZIT
Generic name: SULFUR
Manufacturer: ABBE Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: afed5e8e-324c-44c6-abf6-72938376a4b2
SPL ID: 9a07e62f-1c38-4055-b5ae-b1c06d08dd69
Version: 9
Effective date: 2026-01-13
Source export date: 2026-11-06
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:03:09

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M006	openfda.application_number
brand name		END-ZIT	openfda.brand_name
generic name		SULFUR	openfda.generic_name
manufacturer name		ABBE Laboratories, Inc.	openfda.manufacturer_name
ndc	package	68605-2010-2	openfda.package_ndc
ndc	package	68605-2002-2	openfda.package_ndc
ndc	package	68605-2001-2	openfda.package_ndc
ndc	product	68605-2010	openfda.product_ndc
ndc	product	68605-2002	openfda.product_ndc
ndc	product	68605-2001	openfda.product_ndc
ndc11	package	68605200102	derived:openfda.package_ndc
ndc11	package	68605200202	derived:openfda.package_ndc
ndc11	package	68605201002	derived:openfda.package_ndc
rxcui		422938	openfda.rxcui
rxcui		1094323	openfda.rxcui
spl id		9a07e62f-1c38-4055-b5ae-b1c06d08dd69	id
spl set id		afed5e8e-324c-44c6-abf6-72938376a4b2	set_id
unii		70FD1KFU70	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. • Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor. • Do not get into eyes. If excessive skin irritation deve lops or increases, discontinue use and consult a doctor.

Reported adverse events (FAERS/openFDA)#

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