NEUTROGENA SHEER ZINC 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 mineral sunscreen BROAD SPECTRUM SPF 50

Drug Facts

Active ingredient

Zinc Oxide (21.6%)

Purpose

Sunscreen

Uses

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

Other information

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, Caprylyl Glycol, Cetyl Dimethicone/Bis-Vinyldimethicone Crosspolymer, 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 - 88 mL Tube Label

Neutrogena ®


DERMATOLOGIST RECOMMENDED BRAND

Sheer Zinc

mineral

sunscreen

BROAD SPECTRUM SPF 50

50

100% mineral active

hypoallergenic

water resistant (80 minutes)

3.0 FL OZ (88 mL)

Ntg-001

NEUTROGENA SHEER ZINC MINERAL SUNSCREEN BROAD SPECTRUM SPF 50 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0613
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
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CETYL DIMETHICONE/BIS-VINYLDIMETHICONE CROSSPOLYMER (UNII: AE7QA6TW0Q)  
FEVERFEW (UNII: Z64FK7P217)  
WATER (UNII: 059QF0KO0R)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: X323T6QO4M)  
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0613-5147 mL in 1 TUBE; Type 0: Not a Combination Product01/31/202011/01/2022
2NDC:69968-0613-388 mL in 1 TUBE; Type 0: Not a Combination Product01/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35201/31/2020
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 8/2023
Document Id: 0433b42e-4a93-b1e0-e063-6294a90a3902
Set id: 525f7bae-44b8-44e4-93ea-32995eca2566
Version: 7
Effective Time: 20230831
 
Johnson & Johnson Consumer Inc.