NEUTROGENA PURE AND FREE BABY SUNSCREEN BROAD SPECTRUM SPF 50- zinc oxide lotion 
Kenvue Brands LLC

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Neutrogena ® pure & free ® baby 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 or comments?

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

Distributed by:

Kenvue Brands LLC
Summit, NJ 07901

PRINCIPAL DISPLAY PANEL - 88 mL Tube Label

Neutrogena ®

pure & free ®

baby

SUNSCREEN

Broad Spectrum SPF 50

50

pureSCREEN ®

100% zinc oxide active uva.uvb

ACCEPTED

e

NATIONALECZEMA.ORG

NATIONAL

ECZEMA

ASSOCIATION

TEAR FREE

fragrance free

water resistant

(80 minutes)

#1 DERMATOLOGIST

RECOMMENDED SUNCARE

3.0 FL OZ (88mL)

Neutrogena_1

NEUTROGENA PURE AND FREE BABY  SUNSCREEN BROAD SPECTRUM SPF 50
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0275
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)  
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)  
ETHYL METHICONE (8 MPA.S) (UNII: 3YWG8XYT8H)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CETYL DIMETHICONE/BIS-VINYLDIMETHICONE CROSSPOLYMER (UNII: AE7QA6TW0Q)  
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
GLYCERYL MONOBEHENATE (UNII: A626UU0W2A)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
FEVERFEW (UNII: Z64FK7P217)  
2-ETHYLHEXYL ACRYLATE, METHACRYLATE, METHYL METHACRYLATE, OR BUTYL METHACRYLATE/HYDROXYPROPYL DIMETHICONE COPOLYMER (30000-300000 MW) (UNII: S7ZA3CCJ4M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0275-388 mL in 1 TUBE; Type 0: Not a Combination Product10/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02010/01/2016
Labeler - Kenvue Brands LLC (118772437)

Revised: 3/2025
Document Id: 30c46608-e9a1-a313-e063-6394a90a8a86
Set id: 2d2c58e2-0d15-4383-adae-12fc17b8ea50
Version: 8
Effective Time: 20250320
 
Kenvue Brands LLC