DE LA CRUZ SULFUR ACNE MEDICATION  - sulfur ointment 
DLC Laboratories, Inc.

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De La Cruz Sulfur Ointment 10% Acne Medication

Active Ingredient

Sulfur USP, 10%

Purpose

Acne Medication

Uses

for the treatment of acne

penetrates the pores and dries and clears pimples and blackheads

helps to keep new pimples and blackheads from forming.

Warnings

for external use only

When using this product

do not get into eyes

using other topical acne drugs at the same time or right after 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

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

remove with water

because drying of the skin my occur, start with 1 application daily, then gradually increase to 2 to 3 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 Ingredients

polyethylene glycol

Questions?

1-800-858-3889 or www.dlclabs.com

De La Cruz

SULFUR Ointment 10%

Acne Medication

2.6 ox (73.7g)

Dries and clears pimples and blackheads

Helps to keep new pimples and blackheads from forming

Oil-free, water washable base

No preservatives, artificial colors or fragrances

Manufactured by

De La Cruz Products

A Division of DLC Laboratories, Inc.

Paramount, CA 90723 USA  

Questions: 1-800-858-3989

www.dlclabs.com (c) DLC

DE LA CRUZ SULFUR ACNE MEDICATION  sulfur   ointment

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

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (SULFUR) SULFUR 10 g  in 100 g

Inactive Ingredients Ingredient Name Strength POLYETHYLENE GLYCOL

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 24286-1525-2 73.7 g In 1 JAR None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	02/09/2011

Labeler - DLC Laboratories, Inc. (093351930)

Revised: 03/2011DLC Laboratories, Inc.