Johnsons No More Rash Diaper Rash description, usages, side effects, indications, overdosage, supplying and lots more!

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Johnsons No More Rash Diaper Rash

Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.

Johnson's No More Rash Diaper Rash CreamWith Zinc Oxide3 in 1 Formula


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient(s)

Zinc Oxide 13%

Purpose

Skin Protectant

Uses

  • Helps treat and prevent diaper rash
  • Protects chafed skin due to diaper rash
  • Helps seal out wetness

Warnings

For external use only.

If condition worsens or does not improve within 7 days, consult a physician.

When using this product

  • Avoid contact with eyes

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

Directions

  • Change wet or soiled diapers promptly
  • Clean the diaper area and allow to dry
  • Apply ointment liberally as often as necessary, with each diaper change, especially at bedtime or any time prolonged exposure to wet diapers may be prolonged.

Johnsons No More Rash Diaper Rash Other information

Store between 59-86°F (15-30°C)

Inactive ingredients

Avena sativa (oat) kernel flour, dimethicone, DMDM hydantoin, glycerin, iodopropynyl butylcarbamate, lactic acid, lanolin, magnesium sulfate, microcrystalline wax, mineral oil, panthenol, petrolatum, sodium lactate, sorbitan isostearate, synthetic beeswax, tocopheryl acetate, water

Questions?

1-866-565-2229

Dist. by: Johnson & Johnson CONSUMER PRODUCTS COMPANY
Division of Johnson & Johnson Consumer Companies, Inc.
Skillman, NJ 08558-9418

PRINCIPAL DISPLAY PANEL - 85 g Tube Label

Johnson's®

No More
Rash™

Diaper Rash Cream
With Zinc Oxide

3-in-1
formula

  • helps heal diaper rash
  • forms a protective barrier
  • soothes red, irritated skin

Johnson & Johnson

NET WT 3 OZ (85 g)

Johnsons No More Rash Diaper Rash

Johnsons No More Rash Diaper Rash

Zinc Oxide CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:58232-0212
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 130 mg

Inactive Ingredients

Ingredient Name Strength
Oatmeal
DIMETHICONE
DMDM HYDANTOIN
GLYCERIN
IODOPROPYNYL BUTYLCARBAMATE
LACTIC ACID
LANOLIN
MAGNESIUM SULFATE
MICROCRYSTALLINE WAX
Mineral Oil
PANTHENOL
petrolatum
sodium lactate
Sorbitan Isostearate
ALPHA-TOCOPHEROL ACETATE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:58232-0212-3 85 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part347 2012-04-27


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