DE LA CRUZ SULFUR ACNE MEDICATION- sulfur ointment

De La Cruz Sulfur Acne Medication by

Drug Labeling and Warnings

De La Cruz Sulfur Acne Medication by is a Otc medication manufactured, distributed, or labeled by DLC Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Sulfur, 10%

Purpose

Acne medication

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

Warnings

For external use only

Do not use on

• broken skin
• large areas of the skin

When using this product

• 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

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

Keep out of the reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• 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

polyethylene glycol

Questions?

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 - 73.7 g Jar Label

De La Cruz ®

MAXIMUM STRENGTH

SULFUR
OINTMENT
10%

Acne Medication

2.6 OZ (73.7 g)

INGREDIENTS AND APPEARANCE

DE LA CRUZ SULFUR ACNE MEDICATION 
sulfur ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24286-1525
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24286-1525-2	73.7 g in 1 JAR; Type 0: Not a Combination Product	08/11/2014
2	NDC: 24286-1525-3	2.8 g in 1 POUCH; Type 0: Not a Combination Product	03/17/2015
3	NDC: 24286-1525-4	6 g in 1 JAR; Type 0: Not a Combination Product	03/17/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	08/11/2014

Labeler - DLC Laboratories, Inc. (093351930)

Establishment
Name	Address	ID/FEI	Business Operations
DLC Laboratories, Inc.		093351930	MANUFACTURE(24286-1525) , LABEL(24286-1525)