NEUTROGENA NORWEGIAN FORMULA LIP MOISTURIZER SPF15- octinoxate and oxybenzone lipstick 
Les Emballages Knowlton Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Neutrogena ® NORWEGIAN FORMULA ® Lip Moisturizer SPF 15

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)

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)

Principal Display Panel - 4g Cylinder Blister Pack

NEUTROGENA NORWEGIAN FORMULA LIP MOISTURIZER  SPF15
octinoxate and oxybenzone lipstick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54565-1602
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE40 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CASTOR OIL (UNII: D5340Y2I9G)  
CORN OIL (UNII: 8470G57WFM)  
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54565-1602-21 in 1 BLISTER PACK11/07/2017
1NDC:54565-1602-14 g in 1 CYLINDER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35210/17/2013
Labeler - Les Emballages Knowlton Inc. (248704645)
Establishment
NameAddressID/FEIBusiness Operations
Les Emballages Knowlton Inc.248704645manufacture(54565-1602)

Revised: 11/2017
 
Les Emballages Knowlton Inc.