LUBRIDERM DAILY MOISTURIZER WITH SUNSCREEN SPF15 - avobenzone, octisalate, octocrylene and oxybenzone lotion
Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.

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Lubriderm® Daily Moisture Lotion™
SPF 15

Drug Facts

Active Ingredients	Purpose
Avobenzone (2%)	Sunscreen
Octisalate (4 %)	Sunscreen
Octocrylene (3%)	Sunscreen
Oxybenzone (2.2%)	Sunscreen

Uses

Helps prevent sunburn
Higher SPF gives more sunburn protection
Provides moderate protection against sunburn

Warnings

For external use only.

When using this product

Keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

Rash or irritation develops and lasts.

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

Directions

Apply liberally before sun exposure and as needed.
Children under 6 months of age; ask a doctor.

Other Information

Sun Alert

Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risk of skin aging, skin cancer, and other harmful effects of the sun.

Inactive Ingredients

Water, Glycerin, C12-15 Alkyl Benzoate, Cetyl Alcohol, Glyceryl Stearate, Cetearyl Alcohol, Phenoxyethanol, Ceteareth-20, Stearic Acid, Triethanolamine, Disodium EDTA, Xanthan Gum, Carbomer, Tocopheryl Acetate, Panthenol, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Benzalkonium Chloride, Methylisothiazolinone

Questions?

1-877-543-8477 or visit www.lubriderm.com

PRINCIPAL DISPLAY PANEL - 400 mL Bottle Label

NEW &
IMPROVED

Lubriderm®
dermatologist developed

Daily
Moisture
LOTION

Moisturizer
with Sunscreen
SPF15

15 SPF	WITH BROAD-SPECTRUM UVA/UVB PROTECTION
24	CLINICALLY SHOWN TO MOISTURIZER FOR 24 HOURS

CLEAN, NON-GREASY FEEL

RECOMMENDED
SKIN
CANCER
FOUNDATION

13.5 Fl. Oz. (400 mL)

Principal Display Panel - 400 mL Bottle Label

LUBRIDERM DAILY MOISTURIZER WITH SUNSCREEN SPF15
avobenzone, octisalate, octocrylene, and oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	NDC Product Code (Source)	58232-0718
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Avobenzone (Avobenzone)	Avobenzone	20 mg in 1 mL
Octisalate (Octisalate)	Octisalate	40 mg in 1 mL
Octocrylene (Octocrylene)	Octocrylene	30 mg in 1 mL
Oxybenzone (Oxybenzone)	Oxybenzone	22 mg in 1 mL

Inactive Ingredients
Ingredient Name	Strength
No Inactive Ingredients Found

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	NDC	Package Description	Multilevel Packaging
1	58232-0718-1	400 mL In 1 BOTTLE, PLASTIC	None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part352	06/01/2010

Labeler - Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. (830803164)

Revised: 05/2010Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.