DE LA CRUZ DIAPER RASH- allantoin, petrolatum, and zinc oxide 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.

----------

DE LA CRUZ ®DIAPER RASH OINTMENT

Drug Facts

Active ingredientsPurpose
Allantoin 1%Skin protectant
Petrolatum 45%Skin protectant
Zinc oxide 40%Skin protectant

Uses

Warnings

For external use only.

When using this product

  • do not get into eyes

Stop use and ask a doctor if

  • condition worsens
  • symptoms last for more than 7 days or clear up and occur again within a few days

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

Directions

Other information

Inactive ingredients

alpha-bisabolol, cholecalciferol, lanolin, lavender oil, phenoxyethanol, retinyl palmitate, tocopheryl acetate, purified water, zea mays (corn) starch

Questions

1-800-858-3889

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

PRINCIPAL DISPLAY PANEL - 96 g Tube Label

De La Cruz ®

Baby

Diaper Rash
Ointment

3 in 1
Soothes, Heals, Protects
MAXIMUM
STRENGTH

NET WT 3.4 OZ (96 g) DE LA CRUS DIAPER RASH OINTMENT

DE LA CRUZ DIAPER RASH 
allantoin, petrolatum, and zinc oxide ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1566
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN1 g  in 100 g
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM45 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE40 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
LANOLIN (UNII: 7EV65EAW6H)  
WATER (UNII: 059QF0KO0R)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
STARCH, CORN (UNII: O8232NY3SJ)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
CHOLECALCIFEROL (UNII: 1C6V77QF41)  
LEVOMENOL (UNII: 24WE03BX2T)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24286-1566-21 in 1 CARTON07/10/201511/12/2020
148 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:24286-1566-396 g in 1 TUBE; Type 0: Not a Combination Product12/08/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34707/10/2015
Labeler - DLC Laboratories, Inc. (093351930)
Establishment
NameAddressID/FEIBusiness Operations
DLC Laboratories, Inc.093351930manufacture(24286-1566) , label(24286-1566)

Revised: 6/2023
Document Id: fed071e9-48d3-1462-e053-6394a90a005f
Set id: 5949aa0f-a7cb-453c-81fd-9fa24653a452
Version: 4
Effective Time: 20230623
 
DLC Laboratories, Inc.