Neutrogena Invisible Daily Defense Sunscreen Broad Spectrum SPF 30: Package Insert and Label Information

NEUTROGENA INVISIBLE DAILY DEFENSE SUNSCREEN BROAD SPECTRUM SPF 30- avobenzone, homosalate, octisalate and octocrylene 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 ingredients Purpose
Avobenzone 1.5% Sunscreen
Homosalate 5% Sunscreen
Octisalate 4% Sunscreen
Octocrylene 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 of age: Ask a doctor

Other information

  • protect this product from excessive heat and direct sun
  • May stain some fabrics
  • Store at room temperature

Inactive ingredients

Water, Glycerin, Diisopropyl Adipate, Dimethicone, Alcohol Denat., Silica, Dicaprylyl Carbonate, Caprylyl Methicone, Sodium Acryloyldimethyltaurate/VP Crosspolymer, Polyurethane-62, Pentylene Glycol, Hydroxyacetophenone, Acrylates/Dimethicone Copolymer, Glyceryl Stearate, Phenoxyethanol, Chlorphenesin, Dimethicone Crosspolymer, Fragrance, Tocopheryl Acetate, Disodium EDTA, Sodium Hydroxide, Trideceth-6, Chrysanthemum Parthenium (Feverfew) Flower/Leaf/Stem Juice, Yellow 5, Red 40

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 Label

NEW
Neutrogena ®
#1 DERMATOLOGIST RECOMMENDED BRAND
Invisible Daily
defense

lotion
sunscreen
BROAD SPECTRUM SPF 30
30
sun + environment
oxybenzone free
water resistant (80 minutes)
3.0 FL OZ (88 mL)

PRINCIPAL DISPLAY PANEL -- 88 mL Tube Label
(click image for full-size original)
NEUTROGENA INVISIBLE DAILY DEFENSE SUNSCREEN BROAD SPECTRUM SPF 30
avobenzone, homosalate, octisalate, and octocrylene lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0683
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AVOBENZONE (AVOBENZONE) AVOBENZONE 15 mg in 1 mL
HOMOSALATE (HOMOSALATE) HOMOSALATE 50 mg in 1 mL
OCTISALATE (OCTISALATE) OCTISALATE 40 mg in 1 mL
OCTOCRYLENE (OCTOCRYLENE) OCTOCRYLENE 60 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
GLYCERIN
DIISOPROPYL ADIPATE
DIMETHICONE
ALCOHOL
SILICON DIOXIDE
DICAPRYLYL CARBONATE
CAPRYLYL TRISILOXANE
PENTYLENE GLYCOL
HYDROXYACETOPHENONE
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER
GLYCERYL MONOSTEARATE
PHENOXYETHANOL
CHLORPHENESIN
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE)
.ALPHA.-TOCOPHEROL ACETATE
EDETATE DISODIUM ANHYDROUS
SODIUM HYDROXIDE
TRIDECETH-6
FEVERFEW
FD&C YELLOW NO. 5
FD&C RED NO. 40
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:69968-0683-3 88 mL in 1 TUBE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part352 10/05/2020
Labeler — Johnson & Johnson Consumer Inc. (002347102)

Revised: 01/2021 Johnson & Johnson Consumer Inc.

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