CVS HEALTH DIAPER RASH- zinc oxide cream 
NATURAL ESSENTIALS, 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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Drug Facts

Active ingredient

Zinc Oxide (13%)

Purpose

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 more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

Water, Mineral Oil (Paraffinium Liquidum), Petrolatum, Beeswax, Sorbitan Sesquioleate, Glycerin, Microcrystalline Wax, Dimethicone, Phenoxyethanol, Ethylhexylglycerin, Magnesium Sulfate, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Potassium Hydroxide.

Principal Display Panel – Box Label

CVS

Health®

Compare to the active
ingredient in Desitin® Daily
Defense Diaper Rash Cream*

Cream

Diaper
Rash
Cream

ZINC OXIDE 13%

Skin protectant

Daily use for
diaper rash

Fast acting

Paraben Free

Fragrance free

NET WT 4 OZ (113 g)

Principal Display Panel – Box Label

Principal Display Panel – Tube Label

CVS

Health®

Cream

Diaper
Rash
Cream

ZINC OXIDE 13%

Skin protectant

Daily use for
diaper rash

Fast acting

Paraben Free

Fragrance free

NET WT 4 OZ (113 g)

Principal Display Panel – Tube Label
CVS HEALTH DIAPER RASH 
zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66902-449
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Cation - UNII:13S1S8SF37) Zinc Cation14.7 g  in 113 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
MINERAL OIL (UNII: T5L8T28FGP)  
PETROLATUM (UNII: 4T6H12BN9U)  
WHITE WAX (UNII: 7G1J5DA97F)  
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
GLYCERIN (UNII: PDC6A3C0OX)  
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66902-449-041 in 1 BOX04/01/2020
1113 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34704/01/2020
Labeler - NATURAL ESSENTIALS, INC. (947484713)
Establishment
NameAddressID/FEIBusiness Operations
NATURAL ESSENTIALS, INC.947484713MANUFACTURE(66902-449)

Revised: 4/2020
Document Id: 175b2075-273e-4ae0-9186-094cb2605b4d
Set id: e2a5270e-7c16-47bc-bd19-5652049b4dfd
Version: 1
Effective Time: 20200401
 
NATURAL ESSENTIALS, INC.