CREAMY DIAPER RASH- zinc oxide ointment

Creamy Diaper Rash by

Drug Labeling and Warnings

Creamy Diaper Rash by is a Otc medication manufactured, distributed, or labeled by Geiss, Destin & Dunn, Inc, Vi Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Zinc oxide 13%

purpose

Skin protectant

Uses

• helps treat and prevent diaper rash
• protects chafed skin due to diaper rash and helps seal out wetness

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

change wet and soiled diapers promptly
cleanse the diaper area
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 between  20⁰ and 25⁰ C (68⁰ - 77⁰ F)

Inactive ingredients

water, mineral oil, petrolatum, beeswax, dimethicone, sorbitan sesquioleate, microcrystalline wax, PEG-30 dipolyhydroxystearate, Aloe barbadensis leaf juice, glycerin, tropolone, tocopheryl acetate, 1,2-hexanediol, caprylyl glycol, magnesium sulfate, potassium hydroxide, phenoxyethanol

disclaimer

This product is not manufactured or distributed by Johnson & Johnson Consumer Products Company, distributor of DestineRapid Repid Relief

zince Oxide Diaper Rash Cream

Made in the USA of US and imported parts

Adverse Reactions

Distributed By: Geiss, Destin & Dunn

385 Highway 74 South

Peachtree, GA 30269

www.vlauelabels.com

226.000/226AB

principal display panel

GoodSense

Creamy

Diaper Rash Ointment

Zinc Oxide Skin Protectant

Aloe & Vitamin E Hypoallergenic Goes on smooth and wipes off easily

Compare to Destin Rapid Relief Diaper Rash Cream

Net WT 4 oz (113 g)

INGREDIENTS AND APPEARANCE

CREAMY DIAPER RASH 
zinc oxide ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50804-226
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	13.0 kg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
MINERAL OIL (UNII: T5L8T28FGP)
PETROLATUM (UNII: 4T6H12BN9U)
YELLOW WAX (UNII: 2ZA36H0S2V)
DIMETHICONE (UNII: 92RU3N3Y1O)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
TROPOLONE (UNII: 7L6DL16P1T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
MAGNESIUM SULFATE MONOHYDRATE (UNII: E2L2TK027P)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50804-226-26	113 g in 1 TUBE; Type 0: Not a Combination Product	10/27/1993

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	10/27/1993

Labeler - Geiss, Destin & Dunn, Inc (076059836)

Registrant - Vi Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi Jon		790752542	manufacture(50804-226)