MOISTURE THERAPY INTENSIVE HEALING AND REPAIR SKIN PROTECTANT- petrolatum ointment

Moisture Therapy by

Drug Labeling and Warnings

Moisture Therapy by is a Otc medication manufactured, distributed, or labeled by New Avon LLC, Avon Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient
Petrolatum 60.4%...........................

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

INDICATIONS & USAGE

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

WARNINGS

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.

DOSAGE & ADMINISTRATION

Directions
apply as needed

INACTIVE INGREDIENT

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, TOCOPHEROL, ORYZA SATIVA (RICE) BRAN OIL, HYDROGENATED POLYISOBUTENE, BISABOLOL, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, GLYCINE SOJA (SOYBEAN) STEROLS, LECITHIN, GLYCINE SOJA (SOYBEAN) OIL.

QUESTIONS

Questions? Call 1-800-FOR-AVON

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MOISTURE THERAPY  INTENSIVE HEALING AND REPAIR SKIN PROTECTANT
petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10096-0292
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Petrolatum (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	Petrolatum	604 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10096-0292-1	100 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	09/17/2010

Labeler - New Avon LLC (080143520)

Establishment
Name	Address	ID/FEI	Business Operations
Avon Products, Inc.		005149471	manufacture(10096-0292)