DIAPER RASH- zinc oxide paste

Diaper Rash by

Drug Labeling and Warnings

Diaper Rash by is a Otc medication manufactured, distributed, or labeled by Lidl US, LLC, Vi-Jon, Vi-jon, Memphis Contract Packaging. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Zinc oxide 40%

Purpose

Skin protectant

use

• 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 soilded 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 25⁰C (68⁰ and 77⁰F)

Inactive ingredients

petrolatum, cod liver oil, lanolin, Zea mays (corn) starch, glycerin, sorbitan sesquioleate, beeswax, tocopheryl acetate, fragrance

Disclaimer

This product is not manufactured or distributed by Johnson & Johnson Consumer Products Company, distributor of Destine Maximum Strength 40% Zince Oxide Daiper Rash Paste.

Adverse reaction

DISTRIBUTED BY

Lidl US, LLC

3500 S. Clark Street

Arlington, VA  22202

Lidl

Love It

money refunded

item replaced

020.002/020AC

princpal display panel

Compare to Desitin

Diaper Rash Paste

HYPOALLERGENIC

diaper rash ointment

skin rotectant

40% ZINC OXIDE

paraben, phthalate and

quaternium 15 free

goes on smoothly and

wipes off easily

NET WT 4 OZ (113 g)

INGREDIENTS AND APPEARANCE

DIAPER RASH 
zinc oxide paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71141-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	532 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
COD LIVER OIL (UNII: BBL281NWFG)
LANOLIN (UNII: 7EV65EAW6H)
STARCH, CORN (UNII: O8232NY3SJ)
GLYCERIN (UNII: PDC6A3C0OX)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
YELLOW WAX (UNII: 2ZA36H0S2V)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71141-020-26	1 in 1 CARTON	06/05/2017
1		113 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	06/05/2017

Labeler - Ldl US, LLC (079389709)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-jon		790752542	manufacture(71141-020)

Establishment
Name	Address	ID/FEI	Business Operations
Memphis Contract Packaging		185390010	manufacture(71141-020)