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Johnsons Baby Pure Cornstarch Medicated

Dosage form: powder
Ingredients: Zinc Oxide 100mg in 1g
Labeler: Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
NDC code: 58232-9201

Johnsons Baby Powder Medicated

Drug Facts

Active ingredient

Zinc Oxide 10%

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.

Keep away from face and mouth to avoid inhalation which can cause breathing problems.

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, and allow to dry. Apply powder liberally as often as necessary, with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged.
  • Apply powder close to the body away from child's face. Carefully shake the powder into the diaper or into the hand and apply to the diaper area.

Other Information
  • Do no use if quality seal is broken.
  • Avoid contact with open flame.
  • Close tightly after use.
  • Store at room temperature.

Inactive Ingredients

Zea Mays (Corn) Starch, Fragrance (Aloe Barbadensis Leaf Juice, Tocopheryl (Vitamin E))

Questions?

1-866-JNJ-BABY
(1-866-565-2229)

Distributed in the U.S. by:
JOHNSON & JOHNSON
CONSUMER PRODUCTS
COMPANY
Division of Johnson & Johnson
Consumer Companies, Inc.
Skillman, NJ 08558-9418

PRINCIPAL DISPLAY PANEL - 425 g Bottle Label

CLINICALLY
mildness
PROVEN®

Johnson's®
baby
powder

medicated
zinc oxide skin protectant

3 way action protects,
treats & soothes irritated skin

pure cornstarch

Johnson & Johnson

Net wt. 15 Oz. (425 g)

JOHNSONS BABY PURE CORNSTARCH MEDICATED 
zinc oxide powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58232-9201
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Zinc Oxide (Zinc Oxide) Zinc Oxide100 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN 
ALOE VERA LEAF 
.ALPHA.-TOCOPHEROL 
Packaging
#Item CodePackage Description
1NDC:58232-9201-8425 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34702/04/2014
Labeler - Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. (830803164)

Revised: 05/2015
Document Id: 773de8a9-447a-400d-a1d9-b48005b96ee2
Set id: f5a2734a-9834-439c-b1f0-24fb0e8bcd54
Version: 2
Effective Time: 20150522
 
Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.

Further information

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

Medical Disclaimer