MOISTURE BARRIER- moisture barrier ointment ointment 
Unipack LLC

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Avedana ®Moisture Barrier Ointment (MBO)

Active Ingredient

Active Ingredient

White Petrolatum 98.3%

Purpose

Skin Protectant

Uses

Temporarily protects minor cuts, scrapes, and burns

Temporarily protects and helps relieve chapped or cracked skin

Helps treat and prevent diaper rash caused from wetness, urine and/or stool

Warnings

For external use only

Do not use on

Do not use on - deep or puncture wounds - animal bites - serious burns - an area that is infected

When using this product

When using this product - do not get into eyes

Stop use and ask a doctor if

Stop use and ask a doctor if - condition worsens - symptoms last for more than 7 days or clear up and occur again within a few days

Keep out of reach of children

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Gently cleanse and pat dry affected area

Apply as needed

Inactive ingredients

aloe extract, benzethonium chloride, cholecalciferol (vitamin D), cococaprylate / caprate, corn oil, retinyl palmitate (vitamin A), tocopheryl acetate (vitamin E).

Other information

Protect from freezing.  Avoid excessive heat.

Label

Label

MOISTURE BARRIER 
moisture barrier ointment ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43749-231
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM98.3 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
CORN OIL (UNII: 8470G57WFM)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
CHOLECALCIFEROL (UNII: 1C6V77QF41)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43749-231-0256 g in 1 TUBE; Type 0: Not a Combination Product02/03/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01502/03/2018
Labeler - Unipack LLC (009248480)
Registrant - Unipack LLC (116015769)
Establishment
NameAddressID/FEIBusiness Operations
Unipack LLC009248480manufacture(43749-231)

Revised: 2/2024
Document Id: 11484fca-45ce-e877-e063-6394a90a8bde
Set id: 7a476687-d836-4775-9a8d-b9192b5955a0
Version: 4
Effective Time: 20240213
 
Unipack LLC