Moisture Therapy Ultra Skin Renewal

Dosage form: ointment
Ingredients: Petrolatum 60.3mL in 100mL
Labeler: Avon Products, Inc.
NDC Code: 10096-0228

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.

Drug Facts

Active ingredient
Petrolatum 60.3%...........................

                   Purpose
........................Skin protectant

Uses
• temporarily protects minor: • cuts • scrapes • burns
• helps prevent, temporarily protects and helps relieve chafed,
chapped or cracked skin
• helps prevent and protect from the drying effects of wind and cold
weather

Warnings
For external use only

When using this product
• 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 within
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 right away.

Directions
• apply as needed

Inactive ingredients ETHYLHEXYL PALMITATE, C14-22 ALKANE, CERESIN,
C12-13 ALKYL LACTATE, C18-38 ALKYL HYDROXYSTEAROYL STEARATE,
GLYCERYL CAPRYLATE, BUTYROSPERMUM PARKII (SHEA) BUTTER, HELIANTHUS
ANNUUS (SUNFLOWER) SEED OIL, SALICYLIC ACID, ORYZA SATIVA
(RICE) BRAN OIL, JOJOBA ESTERS, HYDROGENATED POLYISOBUTENE,
BISABOLOL, GLYCINE SOJA (SOYBEAN)
STEROLS, LECITHIN, GLYCINE
SOJA (SOYBEAN) OIL, TOCOPHEROL.

Questions? Call 1-800-FOR-AVON

MOISTURE THERAPY  ULTRA SKIN RENEWAL
petrolatum ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10096-0228
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Petrolatum (PETROLATUM ) Petrolatum60.3 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ETHYLHEXYL PALMITATE  
CERESIN  
GLYCERYL CAPRYLATE  
SALICYLIC ACID  
Packaging
#Item CodePackage Description
1NDC:10096-0228-1100 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34709/17/2010
Labeler - Avon Products, Inc. (001468693)
Establishment
NameAddressID/FEIOperations
Avon Products, Inc.005149471manufacture

Revised: 09/2010
 
Avon Products, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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