Label: AQUASOOTHE ointment

  • NDC Code(s): 67777-555-01, 67777-555-02, 67777-555-03, 67777-555-04, view more
    67777-555-05, 67777-555-06
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 9, 2025

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  • Active ingredient

    Petrolatum 41%

  • Purpose

    Skin Protectant

  • Uses

    • Temporarily protects minor • cuts • scrapes • burns

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

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

  • Warnings

    For external use only

    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 with a few days

    Do not use

    • On deep or puncture wounds • Animal bites • Serious burns

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Other information

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

  • Directions

    Apply as needed

  • Inactive ingredients

    ceresin wax, dexpanthenol, glycerin, lanoline alcohol, mineral oil

  • Questions?

    1-888-DYNAREX Monday - Friday 9AM - 5PM EST

  • Label

    1465_BX_MASTER1465 Label

  • Label

    1464_IN_MASTER1464 Label

  • Label

    1463_IN_MASTER1463 Label

  • INGREDIENTS AND APPEARANCE
    AQUASOOTHE 
    aquasoothe ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-555
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM41 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    MINERAL OIL (UNII: T5L8T28FGP)  
    LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
    DEXPANTHENOL (UNII: 1O6C93RI7Z)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CERESIN (UNII: Q1LS2UJO3A)  
    Product Characteristics
    Color    Score    
    ShapeFREEFORMSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-555-0612 in 1 CASE12/16/2025
    1NDC:67777-555-05144 in 1 BOX
    10.9 g in 1 PACKET; Type 0: Not a Combination Product
    2NDC:67777-555-0412 in 1 CASE12/16/2025
    2NDC:67777-555-03396.9 g in 1 JAR; Type 0: Not a Combination Product
    3NDC:67777-555-0224 in 1 CASE12/16/2025
    3NDC:67777-555-01106 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01612/16/2025
    Labeler - Dynarex Corporation (008124539)
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