QUALITY CHOICE DIAPER RASH- zinc oxide ointment 
Chain Drug Marketing Association 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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Quality Choice Diaper Rash Ointment

Drug Facts

Active Ingredient

Zinc Oxide 40%

Purpose

Skin Protectant

Uses

Keep out of the reach of children.

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

Warnings

For External Use Only

When using this product

This product contains trace amounts of naturally occuring lead.

Directions

Stop use and ask a doctor if

Other Information:

Questions

1-800-935-2362

Inactive Ingredients

BHA, Cod liver oil (high in vitamin A and D), Frangrance, Lanolin, Mineral Oil, Methylparaben, Petrolatum, Purified water, Talc, Tartrazine yellow #4 (FD and C yellow #4)

Helps treat and prevent diaper rash. Protects skin. Relieves Chafing. Promotes Healing

Distributed by:

C.D.M.A., Inc. ©

43157 W 9 Mile Rd

Novi, MI. 48375 USA

www.qualitychoice.com

Product of PRC

Other Information

This product is not manufactured or distributed by Johnson & Johnson Consumer Company Inc. owner of the registered trademark Desitin®.

Packaging

qc diaper rash

QUALITY CHOICE DIAPER RASH 
zinc oxide ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-948
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE40 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
TALC (UNII: 7SEV7J4R1U)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
LANOLIN (UNII: 7EV65EAW6H)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
COD LIVER OIL (UNII: BBL281NWFG)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PETROLATUM (UNII: 4T6H12BN9U)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-948-04113 g in 1 TUBE; Type 0: Not a Combination Product12/19/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34712/19/2019
Labeler - Chain Drug Marketing Association Inc. (011920774)
Registrant - Trifecta Pharmaceuticals USA LLC (079424163)

Revised: 5/2023
Document Id: fc619907-ae29-d730-e053-6394a90a072e
Set id: 9a1184f5-64d8-9786-e053-2a95a90a03b8
Version: 5
Effective Time: 20230523
 
Chain Drug Marketing Association Inc.