MOISTURE THERAPY INTENSIVE HEALING AND REPAIR LIP- octinoxate, oxybenzone 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 Ingredients
Octinoxate 7.5%, Oxybenzone 3.0%..............

            Purpose
................ Sunscreen

INDICATIONS & USAGE

Uses
■ helps prevent sunburn

WARNINGS

WARNINGS
Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

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

DOSAGE & ADMINISTRATION

Directions
apply liberally 15 minutes before sun exposure
children under 6 months of age: ask a doctor
reapply at least every 2 hours
use a water-resistant sunscreen if swimming or sweating

STORAGE AND HANDLING

Other Information
■ protect the product in this container from excessive heat and direct sun.

INACTIVE INGREDIENT

Inactive ingredients: PETROLATUM, ORYZA SATIVA (RICE) BRAN OIL, PARAFFIN, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, HYDROGENATED POLYISOBUTENE, GLYCINE SOJA (SOYBEAN) STEROLS, LECITHIN, GLYCINE SOJA (SOYBEAN) OIL, BENZYL ALCOHOL, BHT.

QUESTIONS

Questions? 1-800-FOR-AVON

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MOISTURE THERAPY  INTENSIVE HEALING AND REPAIR LIP
octinoxate, oxybenzone ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10096-0103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	30 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10096-0103-1	15 mL in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	05/22/2012

Labeler - New Avon LLC (080143520)

Establishment
Name	Address	ID/FEI	Business Operations
Avon Products, Inc.		005149471	manufacture(10096-0103)