Diaper Rash description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Diaper Rash

Dolgencorp, LLC
Vi-Jon

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

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

Diaper Rash Other information

store between 20⁰ and 25 ⁰C (68 ⁰ and 77 ⁰F)

Inactive ingredients

BHA, cod liver oil, fragance, lanolin, petrolatum, phenoxyethanol, talc, water

Questions?

Call 1-888-309-9030

Disclaimer

This product is not manufactured or distributed by Johnson + Johnson Consumer Products Company, distributor of Destine Maximum Strength Daiper Rash Paste.

Adverse reaction

DISTRIBUTED BY

DOLGENCORP, LLC

100 MISSION RIDGE

GOODLETTSVILLE, TN

37072

100%

Quality

Guaranteed

(888)309-9030

Principal Display Panel

DG baby

Maximum Strength

Diaper Rash

Ointment

Skin Protectant/Zinc oxide 40%

Quaternium-15 + Paraben Free

  • Helps heal, soothe + prevent diaper rash

Compare to Destine Maximum Strength Diaper Rash Paste

NET WT 4 OZ (113 g)

Diaper Rash

Diaper Rash

Zinc oxide PASTE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:55910-020
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 532 mg

Inactive Ingredients

Ingredient Name Strength
BUTYLATED HYDROXYANISOLE
COD LIVER OIL
LANOLIN
petrolatum
PHENOXYETHANOL
talc
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 113 in 1 TUBE
2 NDC:55910-020-26 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part347 2012-05-10


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.