Neutrogena Age Shield Face Oil Free Sunscreen Broad Spectrum SPF 110: Package Insert and Label Information

NEUTROGENA AGE SHIELD FACE OIL FREE SUNSCREEN BROAD SPECTRUM SPF 110- 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.

Drug Facts

Active ingredient Purpose
Avobenzone (3%) Sunscreen
Homosalate (15%) Sunscreen
Octisalate (5%) Sunscreen
Octocrylene (10%) Sunscreen
Oxybenzone (6%) Sunscreen

Uses

  • 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 15 minutes before sun exposure
  • reapply:
    • after 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 SPF value 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, Fragrance, Chlorphenesin, Triethanolamine, Diethylhexyl 2,6-Naphthalate, Dipotassium Glycyrrhizate, Disodium EDTA, BHT, Methylisothiazolinone

Questions?

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

Distributed by: JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL — 88 mL Tube Carton

Neutrogena ®
#1 DERMATOLOGIST RECOMMENDED BRAND
Age Shield ®
Face

oil-free

sunscreen
BROAD SPECTRUM SPF 110
110

helioplex ®
broad spectrum uva•uvb

shields skin 6-layers deep
from skin-aging UVA rays
water resistant (80 minutes)

3.0 FL OZ (88mL)

PRINCIPAL DISPLAY PANEL -- 88 mL Tube Carton
(click image for full-size original)
NEUTROGENA AGE SHIELD FACE OIL FREE SUNSCREEN BROAD SPECTRUM SPF 110
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0611
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AVOBENZONE (AVOBENZONE) AVOBENZONE 30 mg in 1 mL
HOMOSALATE (HOMOSALATE) HOMOSALATE 150 mg in 1 mL
OCTISALATE (OCTISALATE) OCTISALATE 50 mg in 1 mL
OCTOCRYLENE (OCTOCRYLENE) OCTOCRYLENE 100 mg in 1 mL
OXYBENZONE (OXYBENZONE) OXYBENZONE 60 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER
SILICON DIOXIDE
YELLOW WAX
CYCLOMETHICONE 5
ETHYLHEXYLGLYCERIN
GLYCERYL MONOSTEARATE
PEG-100 STEARATE
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
CHLORPHENESIN
TROLAMINE
DIETHYLHEXYL 2,6-NAPHTHALATE
GLYCYRRHIZINATE DIPOTASSIUM
EDETATE DISODIUM ANHYDROUS
BUTYLATED HYDROXYTOLUENE
METHYLISOTHIAZOLINONE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:69968-0611-3 1 TUBE in 1 CARTON contains a TUBE
1 88 mL in 1 TUBE This package is contained within the CARTON (69968-0611-3)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part352 01/31/2020
Labeler — Johnson & Johnson Consumer Inc. (002347102)

Revised: 04/2021 Johnson & Johnson Consumer Inc.

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