Neutrogena® Sheer Zinc Face mineral sunscreen BROAD SPECTRUM SPF 50

Neutrogena® Sheer Zinc Face mineral sunscreen BROAD SPECTRUM SPF 50

Drug Labeling and Warnings

Drug Details

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NEUTROGENA SHEER ZINC FACE MINERAL SUNSCREEN BROAD SPECTRUM SPF 50- zinc oxide 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.

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Neutrogena® Sheer Zinc Face mineral sunscreen BROAD SPECTRUM SPF 50

Drug Facts

Active ingredient

Zinc Oxide (21.6%)

Purpose

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

Inactive ingredients

Water, C12-15 Alkyl Benzoate, Styrene/Acrylates Copolymer, Octyldodecyl Citrate Crosspolymer, Phenyl Trimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Dimethicone, Glycerin, Polyhydroxystearic Acid, Ethyl Methicone, Silica, Cetyl Dimethicone, Triethoxycaprylylsilane, Phenoxyethanol, Glyceryl Behenate, Sodium Chloride, Acrylates/Dimethicone Copolymer, Chlorphenesin, Phenethyl Alcohol, Avena Sativa (Oat) Kernel Flour, Caprylyl Glycol, Cetyl Dimethicone/Bis-Vinyldimethicone Crosspolymer, Tocopheryl Acetate, Chrysanthemum Parthenium (Feverfew) Flower/Leaf/Stem Juice

Questions?

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

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 59 mL Tube Carton

Neutrogena®
#1 DERMATOLOGIST RECOMMENDED BRAND

Sheer Zinc
Face
mineral
sunscreen
BROAD SPECTRUM SPF 50
50

100% mineral active
hypoallergenic
oil free
water resistant (80 minutes)

2.0 FL OZ (59mL)

Principal Display Panel - 59 mL Tube Carton
NEUTROGENA SHEER ZINC FACE MINERAL SUNSCREEN BROAD SPECTRUM SPF 50 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 69968-0623
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide216 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)  
Phenyl Trimethicone (UNII: DR0K5NOJ4R)  
Dimethicone (UNII: 92RU3N3Y1O)  
Glycerin (UNII: PDC6A3C0OX)  
ETHYL METHICONE (8 MPA.S) (UNII: 3YWG8XYT8H)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
Triethoxycaprylylsilane (UNII: LDC331P08E)  
Phenoxyethanol (UNII: HIE492ZZ3T)  
GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)  
Sodium Chloride (UNII: 451W47IQ8X)  
Chlorphenesin (UNII: I670DAL4SZ)  
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)  
OATMEAL (UNII: 8PI54V663Y)  
Caprylyl Glycol (UNII: 00YIU5438U)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
FEVERFEW (UNII: Z64FK7P217)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 69968-0623-21 in 1 CARTON01/31/2020
159 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 finalpart35201/31/2020
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 12/2019
 
Johnson & Johnson Consumer Inc.


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