NEUTROGENA ULTRA SHEER FACE AND BODY  SUNSCREEN BROAD SPECTRUM SPF70- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone stick 
Johnson & Johnson Consumer 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 Ultra Sheer Face & Body Stick Sunscreen Broad Spectrum SPF 70

Drug Facts

Active ingredients

Avobenzone 3%
Homosalate 15%
Octisalate 5%
Octocrylene 10%
Oxybenzone 3%

Purpose

Sunscreen

Use

  • Helps prevent sunburn
  • If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

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
  • ensure complete coverage to the area above the lip, nose, and tops of ears.
  • reapply:
    • 80 minutes of swimming or sweating
    • immediately after towel drying
    • at least every 2 hours
  • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum value of SPF of 15 or higher and other sun protection measures including:
    • Limit time in the sun, especially from 10 a.m. – 2 p.m.
    • Wear long-sleeve shirts, pants hats, and sunglasses
  • 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

Adipic Acid/Diglycol Crosspolymer, Beeswax, BHT, C12-15 Alkyl Benzoate, Caprylyl Glycol, Diethylhexyl 2,6-Naphthalate, Fragrance, Neopentyl Glycol Diethylhexanoate, Neopentyl Glycol Diisostearate, Octyldodecyl Neopentanoate, Ozokerite, Paraffin, Polyethylene, Silica

Questions or comments?

Call toll-free 800-299-4786 or 215-273-8755 (collect) or visit www.neutrogena.com

Dist. by
Neutrogena Corp.
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 42 g Cylinder Label

Neutrogena®

NEW
Ultra Sheer®
FACE & BODY STICK
SUNSCREEN

Broad Spectrum SPF 70

70
helioplex®
broad spectrum uva•uvb

#1 DERMATOLOGIST
RECOMMENDED SUNCARE

NET WT 1.5 OZ (42g)

Principal Display Panel - 42 g Cylinder Label
NEUTROGENA ULTRA SHEER FACE AND BODY   SUNSCREEN BROAD SPECTRUM SPF70
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10812-419
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone30 mg  in 1 g
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S) Homosalate150 mg  in 1 g
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate50 mg  in 1 g
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene100 mg  in 1 g
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone30 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Yellow Wax (UNII: 2ZA36H0S2V)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
Diethylhexyl 2,6-Naphthalate (UNII: I0DQJ7YGXM)  
Neopentyl Glycol Diethylhexanoate (UNII: U68ZV6W62C)  
Neopentyl Glycol Diisostearate (UNII: 4M6OQ34JWW)  
Octyldodecyl Neopentanoate (UNII: X8725R883T)  
Paraffin (UNII: I9O0E3H2ZE)  
High Density Polyethylene (UNII: UG00KM4WR7)  
Silicon Dioxide (UNII: ETJ7Z6XBU4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10812-419-0242 g in 1 CYLINDER; Type 0: Not a Combination Product09/05/201310/26/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35209/05/201310/26/2018
Labeler - Johnson & Johnson Consumer Inc. (002347102)
Registrant - Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. (830803164)

Revised: 10/2017
Document Id: 4e5c3e95-7ac2-4fd3-a4fe-62956b52405f
Set id: 651d8cd1-f92e-4547-bc22-8bebc8d150bc
Version: 4
Effective Time: 20171030
 
Johnson & Johnson Consumer Inc.