LUBRIDERM - avobenzone, homosalate, octisalate, oxybenzone and octocrylene lotion 
Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.

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Lubriderm Advanced Therapy Moisturizing Lotion SPF 30

Drug Facts

Active Ingredients	Purpose
Avobenzone 3%	Sunscreen
Homosalate 6%	Sunscreen
Octisalate 5%	Sunscreen
Oxybenzone 5%	Sunscreen
Octocrylene 4%	Sunscreen

Uses

• Helps prevent sunburn
• Higher SPF gives more sunburn protection
• Provides high 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, C12-15 Alkyl Benzoate, Hydroxypropyl Starch Phosphate, Cetearyl Alcohol, Glycerin, Distearyldimonium Chloride, Stearyl Alcohol, Ceteareth-20, Fragrance, Linum Usitatissimum (Linseed) Seed Oil, Panthenol, Tocopheryl Acetate, Disodium EDTA, Rosmarinus Officinalis (Rosemary) Leaf Extract, Methylisothiazolinone

Questions?

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

PRINCIPAL DISPLAY PANEL - 28g Carton

Lubriderm®
dermatologist developed

Advanced
Therapy
LOTION ™

Moisturizer
with Sunscreen
SPF 30
HYDRATES EXTRA-DRY SKIN
LONG-LASTING UVA/UVB PROTECTION
NON-GREASY

Net Wt. 1 Oz. (28g)

LUBRIDERM  avobenzone, homosalate, octisalate, oxybenzone and octocrylene   lotion

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 58232-0748 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (Avobenzone) Avobenzone 30 mg  in 1 g Homosalate (Homosalate) Homosalate 60 mg  in 1 g Octisalate (Octisalate) Octisalate 50 mg  in 1 g Oxybenzone (Oxybenzone) Oxybenzone 50 mg  in 1 g Octocrylene (Octocrylene) Octocrylene 35.5 mg  in 1 g

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 58232-0748-8 227 g In 1 TUBE None 2 58232-0748-6 28 g In 1 TUBE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	03/30/2010

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

Revised: 03/2010Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.