WHITE PETROLATUM- petrolatum ointment 
Dynarex Corporation

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1140 White Petrolatum NDC 67777-005-00

1141 White Petrolatum NDC 67777-005-10

1145 White Petrolatum NDC 67777-005-50

1147 White Petrolatum NDC 67777-005-70

Active Ingredient

White Petrolatum 100%

Purpose

Skin Protectant

Uses

• Temporarily protects minor cuts, scrapes, burns

• Temporarily protects and helps relieve chafed, chapped, or cracked skin and lips

• Helps prevent and protect from the drying effects of wind and cold weather

• Protects chafed skin due to diaper rash

Warnings

For external use only

Do not use on

• Deep or puncture wounds

• Animal bites

• Serious burns

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 (1-800-222-12222) 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 other uses: Apply as needed.

Other Information

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

• Avoid excessive heat

• Tamper evident. Do not use if seal is torn, cut, or opened

Questions?

1-888-396-2739 Monday - Friday, 9AM - 5PM EST.

Inactive Ingredient

Label

1140 BX MASTER1140 White Petrolatum

Label

1140 BX GVIN0101140 White Petrolatum

Label

1141 BX MASTER1141 White Petrolatum

Label

1147 IN MASTER1147 White Petrolatum

Label

1145 BX MASTER1145 White Petrolatum

WHITE PETROLATUM 
petrolatum ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WHITE PETROLATUM (UNII: B6E5W8RQJ4) (WHITE PETROLATUM - UNII:B6E5W8RQJ4) WHITE PETROLATUM1 g  in 1 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67777-005-00864 in 1 CASE10/26/2018
1NDC:67777-005-01144 in 1 BOX
15 g in 1 PACKET; Type 0: Not a Combination Product
2NDC:67777-005-1072 in 1 CASE10/26/2018
2NDC:67777-005-111 in 1 BOX
228.4 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:67777-005-5072 in 1 CASE10/26/2018
3NDC:67777-005-516 in 1 BOX
3113 g in 1 TUBE; Type 0: Not a Combination Product
4NDC:67777-005-7012 in 1 CASE10/26/2018
4NDC:67777-005-71425 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01610/26/2018
Labeler - Dynarex Corporation (008124539)

Revised: 1/2024
Document Id: 101cf675-7af4-0376-e063-6294a90a5e9d
Set id: 81f5092d-0632-bf47-e053-2991aa0ac563
Version: 10
Effective Time: 20240129
 
Dynarex Corporation