AQUASOOTHE- aquasoothe ointment 
Dynarex Corporation

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1463 AquaSoothe
1464 Aqua Soothe
1465 Aqua Soothe

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

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)

Revised: 12/2025
Document Id: 45878c3c-d05e-984c-e063-6294a90a4661
Set id: 45878c3c-d05d-984c-e063-6294a90a4661
Version: 1
Effective Time: 20251209
 
Dynarex Corporation