NEUTROGENA AGE SHIELD FACE OIL FREE  SUNSCREEN BROAD SPECTRUM SPF110- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion 
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.

----------

Neutrogena Age Shield Face Oil-Free Lotion Sunscreen Broad Spectrum SPF 110

Drug Facts

Active ingredients

Avobenzone 3%
Homosalate 15%
Octisalate 5%
Octocrylene 10%
Oxybenzone 6%

Purpose

Sunscreen

Uses

  • Helps prevent sunburn
  • (Optional) 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 15 minutes before sun exposure
  • reapply:
    • after 40 minutes [or 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-sleeved shirts, pants hats, and sunglasses
  • Children under 6 months: Ask a doctor

Other information

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

Inactive Ingredients

Water, Styrene/Acrylates Copolymer, Silica, Beeswax, Cyclopentasiloxane, Ethylhexylglycerin, Glyceryl Stearate, PEG-100 Stearate, Acrylates/Dimethicone Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Chlorphenesin, Disodium EDTA, Triethanolamine, Dipotassium Glycyrrhizate, BHT, Methylisothiazolinone, Diethylhexyl 2,6-Naphthalate, Fragrance

Questions or comments?

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

PRINCIPAL DISPLAY PANEL - 88mL Tube Carton

Neutrogena®
Age Shield
face
oil-free lotion
SUNSCREEN
Broad Spectrum
SPF 110

helioplex®
broad spectrum uva•uvb

RECOMMENDED
Skin
Cancer
Foundation
RECOMMENDED
AS AN EFFECTIVE
UV SUNSCREEN
SUPERIOR ANTI-AGING
PROTECTION
shields skin 6-layers deep
from skin-aging UVA rays

water resistant
(80 minutes)

#1 DERMATOLOGIST
RECOMMENDED SUNCARE

3.0 FL OZ (88mL)

PRINCIPAL DISPLAY PANEL - 88mL Tube Carton
NEUTROGENA AGE SHIELD FACE OIL FREE   SUNSCREEN BROAD SPECTRUM SPF110
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10812-427
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone30 mg  in 1 mL
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S) Homosalate150 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate50 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene100 mg  in 1 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone60 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Silicon Dioxide (UNII: ETJ7Z6XBU4)  
Yellow Wax (UNII: 2ZA36H0S2V)  
Cyclomethicone 5 (UNII: 0THT5PCI0R)  
Ethylhexylglycerin (UNII: 147D247K3P)  
Glyceryl Monostearate (UNII: 230OU9XXE4)  
PEG-100 Stearate (UNII: YD01N1999R)  
Chlorphenesin (UNII: I670DAL4SZ)  
Edetate Disodium (UNII: 7FLD91C86K)  
Trolamine (UNII: 9O3K93S3TK)  
Glycyrrhizinate Dipotassium (UNII: CA2Y0FE3FX)  
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)  
Methylisothiazolinone (UNII: 229D0E1QFA)  
Diethylhexyl 2,6-Naphthalate (UNII: I0DQJ7YGXM)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10812-427-011 in 1 CARTON10/16/201203/25/2022
188 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35210/16/201203/25/2022
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 4/2020
Document Id: 05242e71-b696-4735-b70f-3ac71371eb91
Set id: 8890374d-42a8-4113-917a-b0e17d70d059
Version: 3
Effective Time: 20200422
 
Johnson & Johnson Consumer Inc.