Acne Treatment with Sulfur

Manufacturer: DLC Laboratories, Inc.
Effective date: 2026-01-07
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 01:31:49

Label at a glance#

ProductAcne Treatment with Sulfur

Active ingredientSULFUR

Label structure10 sections

Indications and uses

for the treatment of acne penetrates the pores and dries and clears acne pimples and blackheads helps to keep new acne pimples and blackheads from forming

Dosage and administration

cleanse the skin thoroughly before applying cover the entire affected area with a thin layer leave on for 10 minutes thoroughly remove with water because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to three times daily if needed or as directed by a doctor if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Contacts and useful links#

PhoneLabel contact1-800-858-3889

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sulfur, 5%

Purpose

OTC - PURPOSE SECTION

Acne medication

Uses

INDICATIONS & USAGE SECTION

for the treatment of acne

penetrates the pores and dries and clears acne pimples and blackheads
helps to keep new acne pimples and blackheads from forming

Warnings

WARNINGS SECTION

For external use only

Do not use on

OTC - DO NOT USE SECTION

broken skin
large areas of the skin

When using this product

OTC - WHEN USING SECTION

do not get into eyes
skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time or right after use of this product. If irritation occurs, only use one topical acne medication at a time.
apply only to areas with acne

OTC - STOP USE SECTION

Stop use and consult a doctor ifexcessive skin irritation develops or increases.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

cleanse the skin thoroughly before applying
cover the entire affected area with a thin layer
leave on for 10 minutes
thoroughly remove with water
because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to three times daily if needed or as directed by a doctor
if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Inactive ingredient

INACTIVE INGREDIENT SECTION

polyethylene glycol

Questions

OTC - QUESTIONS SECTION

1-800-858-3889

SPL UNCLASSIFIED SECTION

Manufactured by: De La Cruz Products
A Division of DLC Laboratories, Inc. | Paramount, CA 90723 USA

PRINCIPAL DISPLAY PANEL - 74 g Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

De La Cruz _®

FOR SENSITIVE SKIN

ACNE
TREATMENT

With 5% Sulfur

Antibacterial & Anti-inflammatory
Clears & Helps Prevent Acne

OIL-FREE
WATER-WASHABLE

Ointment

2.6 OZ (74 g)

Acne treatment 5% sulfur

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
417863	sulfur 5 % Topical Ointment	PSN	5
417863	sulfur 0.05 MG/MG Topical Ointment	SCD	5
417863	sulfur 5 % Topical Ointment	SY	5

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0324286154609	GTIN-13: 0324286154609 EAN-13: 0324286154609 GTIN-12: 324286154609 UPC-A: 324286154609 GTIN storage (14 digits): 00324286154609	Acne-02.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
d723478e-ad4a-ec23-6bd7-cfe33e1e3840	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
24286-1573-1	Acne Treatment with Sulfur	74 g in 1 TUBE	OINTMENT	74		5
24286-1573-2	Acne Treatment with Sulfur	6 g in 1 JAR	OINTMENT	6		5

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

Acne Treatment with Sulfur
SULFUR
POLYETHYLENE GLYCOL 400
POLYETHYLENE GLYCOL 3350

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
24286-1573	24286-1573-1, 24286-1573-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
POLYETHYLENE GLYCOL 400	B697894SGQ	IACT
POLYETHYLENE GLYCOL 3350	G2M7P15E5P	IACT
SULFUR	70FD1KFU70	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Acne Treatment with Sulfur	SULFUR	DLC Laboratories, Inc.	aa1f2afe-7b09-4448-b522-e1b23d63d3ef	2026-01-07	Warnings	Exact identifier ndc (package): 24286-1573-1 ndc (package): 24286-1573-2 ndc (product): 24286-1573 ndc11 (package): 24286157302 ndc11 (package): 24286157301 spl id: 47d54c4e-039b-d2de-e063-6294a90ade7b spl set id: aa1f2afe-7b09-4448-b522-e1b23d63d3ef

Reported adverse events (FAERS/openFDA)#

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