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WESTERN FAMILY DIAPER RASH

Medically reviewed on Oct 5, 2018

Dosage form: ointment
Ingredients: ZINC OXIDE 0.40g in 1g
Labeler: TAI GUK PHARM. CO., LTD.
NDC Code: 68169-0375

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.

Drug Facts

Active Ingredient                                                                        Purpose

Zinc oxide, 40% ........................................................................Skin protectant

Uses

  • helps treat and prevent diaper rash
  • protects chafed skin due to diaper rash and helps protect skin from wetness
  • helps prevent and temporarily protect chafed, chapped, cracked or windburned skin and lips

For external use only

Do not use over deep or puncture wounds, infections or lacerations

When using this product avoid contact with the eyes

Stop use and ask a doctor if condition worsens or does not improve within 7 days

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

Directions

  • change wet and soiled diapers promptly, cleanse the diaper area and allow to dry
  • apply ointment liberally as often as necessary, with each diaper change especially at bedtime or anytime when exposure to wet diapers may be prolonged

Other information

  • store at 20o to 25oC (68o to 77oF)
  • Lot No. and Exp. Date: see box or see crimp of tube

Inactive ingredients

BHA, cod liver oil (high in vitamins A and D), fragrance, lanolin, light mineral oil, methylparaben, petrolatum, purified water, talc, tartrazine yellow #4 (FD and C yellow #4)

Proudly Distributed By:

Western Family Foods, Inc.

P.O. Box 4057, Portland, OR 97208 U.S.A.

Copyright 2010 Marca Registrada

www.westernfamily.com

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WESTERN FAMILY DIAPER RASH 
zinc oxide ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68169-0375
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE0.40 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
COD LIVER OIL 
LANOLIN 
LIGHT MINERAL OIL 
METHYLPARABEN 
PETROLATUM 
WATER 
TALC 
Packaging
#Item CodePackage Description
1NDC:68169-0375-41 TUBE (TUBE) in 1 CARTON
156 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34710/05/2010
Labeler - TAI GUK PHARM. CO., LTD. (631101656)
Registrant - UNITED EXCHANGE CORP. (840130579)
Establishment
NameAddressID/FEIOperations
TAI GUK PHARM. CO., LTD.631101656manufacture

 
TAI GUK PHARM. CO., LTD.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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