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

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.

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DE LA CRUZ ® SULFUR ACNE MEDICATION

Drug Facts

Active ingredient

Sulfur, 10%

Purpose

Acne medication

Uses

for the treatment of acne

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

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)

PRINCIPAL DISPLAY PANEL - 73.7 g Jar Label
DE LA CRUZ SULFUR ACNE MEDICATION 
sulfur ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1525
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR10 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24286-1525-273.7 g in 1 JAR; Type 0: Not a Combination Product08/11/201403/26/2021
2NDC:24286-1525-32.8 g in 1 POUCH; Type 0: Not a Combination Product03/17/201512/06/2021
3NDC:24286-1525-46 g in 1 JAR; Type 0: Not a Combination Product03/17/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D08/11/2014
Labeler - DLC Laboratories, Inc. (093351930)
Establishment
NameAddressID/FEIBusiness Operations
DLC Laboratories, Inc.093351930manufacture(24286-1525) , label(24286-1525)

Revised: 12/2021
Document Id: d282404b-2979-316d-e053-2995a90aea2c
Set id: c00d53c4-a150-411f-acd7-4ffb8a35d449
Version: 8
Effective Time: 20211206
 
DLC Laboratories, Inc.