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De La Cruz Sulfur Acne Medication

Dosage form: ointment
Ingredients: SULFUR 10g in 100g
Labeler: DLC Laboratories, Inc.
NDC Code: 24286-1525

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

DE LA CRUZ ® SULFUR ACNE MEDICATION

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

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)

DE LA CRUZ SULFUR ACNE MEDICATION 
sulfur ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1525
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SULFUR (SULFUR) SULFUR10 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
POLYETHYLENE GLYCOLS 
Packaging
#Item CodePackage Description
1NDC:24286-1525-273.7 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D08/11/2014
Labeler - DLC Laboratories, Inc. (093351930)
Establishment
NameAddressID/FEIOperations
DLC Laboratories, Inc.093351930MANUFACTURE(24286-1525), LABEL(24286-1525)

Revised: 01/2015
 
DLC Laboratories, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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