ZINC OXIDE- zinc oxide ointment ointment 
Dynarex Corporation

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1190, 1191, 1192 Zinc Oxide Ointment 20%

Active Ingredient

Zinc Oxide 20%

Purpose

Skin Protectant

Use(s)

• Helps treat chafed skin associated with diaper rash

• Dries the oozing and weeping of poison ivy, oak, and sumac

Warnings

For External Use Only

When using this product

• Avoid contact with 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 (1-800-222-1222) right away.

Directions

• For diaper rash: Change wet and soiled diapers promptly, cleanse the diaper area, and 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.

• For poison ivy, oak, and sumac: Apply as needed.

Other Information

• Store at room temperature between 15º-30ºC (59º-86ºF)

• Avoid excessive heat

• Tamper evident. Do not use if seal is damaged.

Inactive Ingredients

Cetomacrogol 1000. Cetostearyl Alcohol Light Liquid Paraffin, White Soft Paraffin

Questions?

1-888-Dynarex Monday - Friday, 9AM - 5PM EST.

Label

1192_IN_MASTERLabel 1192

Label

1190_BX_MASTERLabel 1190

Label

1191_BX_MASTERLabel 1191

ZINC OXIDE 
zinc oxide ointment ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-223
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE200 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WHITE PETROLATUM (UNII: B6E5W8RQJ4)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
CETETH-20 (UNII: I835H2IHHX)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
Product Characteristics
Color    Score    
ShapeFREEFORMSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67777-223-0272 in 1 CASE02/29/2024
1NDC:67777-223-111 in 1 BOX
1NDC:67777-223-0128.4 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:67777-223-0472 in 1 CASE02/29/2024
2NDC:67777-223-131 in 1 BOX
2NDC:67777-223-0356.7 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:67777-223-0612 in 1 CASE02/29/2024
3NDC:67777-223-05425 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01602/29/2024
Labeler - Dynarex Corporation (008124539)

Revised: 2/2024
Document Id: 11d79dd6-35f8-4399-e063-6294a90ac7dd
Set id: 11d79dd6-35f7-4399-e063-6294a90ac7dd
Version: 1
Effective Time: 20240220
 
Dynarex Corporation