SKIN PROTECTANT PETROLATUM- petrolatum ointment 
Nationwide Pharmaceutical, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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SKIN PROTECTANT PETROLATUM OINTMENT

Drug Facts

Active ingredient

Petrolatum 44.28%

Purpose

Skin protectant

Uses

Warnings

For external use only.

When using this product

  • do not get into eyes In case of contact, flush thoroughly with water.

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.

Do not use on

  • deep or puncture wounds
  • animal bites
  • serious burns
  • broken skin

Keep out of reach of children. In case of accidental ingestion contact a physician or Poison Control Center right away.

Directions

Apply as needed.

Other information

Inactive ingredients

cetostearyl alcohol, microcrystalline wax, mineral oil, and polysorbate 60

Questions or comments?

1-800-697-3329

PRINCIPAL DISPLAY PANEL - 454 GM Jar Label

NDC 69375-0004-54

Nationwide
Pharmaceutical

Skin Protectant
Petrolatum Ointment

For dry, cracked or irritated skin

454 GM (16 OZ)

PRINCIPAL DISPLAY PANEL - 454 GM Jar Label
SKIN PROTECTANT PETROLATUM 
petrolatum ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69375-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Petrolatum (UNII: 4T6H12BN9U) (Petrolatum - UNII:4T6H12BN9U) Petrolatum44.28 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
MINERAL OIL (UNII: T5L8T28FGP)  
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69375-004-54454 g in 1 JAR; Type 0: Not a Combination Product03/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34703/01/2021
Labeler - Nationwide Pharmaceutical, LLC (079265801)

Revised: 2/2021
Document Id: 21aaf4fe-9205-4f02-90c5-e00982dba6e5
Set id: e38d1050-df08-4b18-b4e4-11688ca2bedc
Version: 1
Effective Time: 20210223
 
Nationwide Pharmaceutical, LLC