NEUTROGENA NORWEGIAN FORMULA LIP MOISTURIZER SPF15- octinoxate and oxybenzone lipstick

Neutrogena Norwegian Formula Lip Moisturizer by

Drug Labeling and Warnings

Neutrogena Norwegian Formula Lip Moisturizer by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredients

Octinoxate 7.5%
Oxybenzone 4%

Purpose

Sunscreen

Use

• Helps prevent sunburn

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.

Directions

• apply liberally and evenly 15 minutes before sun exposure.
• use a water resistant sunscreen if swimming or sweating
• reapply at least every 2 hours
• Children under 6 months of age: Ask a doctor

Other information

• Protect this product from excessive heat and direct sun
• May stain some fabrics

Inactive Ingredients

Castor (Ricinus Communis) Seed Oil
Corn (Zea Mays) Oil
Ozokerite
Petrolatum
Beeswax
Ethylhexyl Palmitate
Paraffin
Stearyl Alcohol
Carnauba (Copernicia Cerifera) Wax
BHT

Questions or comments?

Visit www.neutrogena.com or call toll-free 800-582-4048 or 215-273-8755 (collect)

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Dist. by Neutrogena Corp.
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 4g Cylinder Blister Pack

NORWEGIAN
FORMULA®

lip moisturizer
SUNSCREEN
SPF 15

conditions and protects dry lips

Neutrogena®

DERMATOLOGIST RECOMMENDED

NET WT. 0.15 OZ. (4g)

INGREDIENTS AND APPEARANCE

NEUTROGENA NORWEGIAN FORMULA LIP MOISTURIZER   SPF15
octinoxate and oxybenzone lipstick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10812-874
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 g
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y)	Oxybenzone	40 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
castor oil (UNII: D5340Y2I9G)
Corn oil (UNII: 8470G57WFM)
ceresin (UNII: Q1LS2UJO3A)
petrolatum (UNII: 4T6H12BN9U)
yellow wax (UNII: 2ZA36H0S2V)
ethylhexyl palmitate (UNII: 2865993309)
paraffin (UNII: I9O0E3H2ZE)
stearyl alcohol (UNII: 2KR89I4H1Y)
carnauba wax (UNII: R12CBM0EIZ)
butylated hydroxytoluene (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10812-874-01	1 in 1 BLISTER PACK	10/17/2013
1		4 g in 1 CYLINDER; 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	10/17/2013

Labeler - Johnson & Johnson Consumer Inc. (002347102)