NEUTROGENA CLEAR FACE BREAKOUT FREE OIL FREE BROAD SPECTRUM SPF 55- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion 
Johnson & Johnson Consumer Inc.

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Neutrogena ® clear face BREAK-OUT FREE liquid-lotion SUNSCREEN Broad Spectrum SPF 55

Drug Facts

Active IngredientsPurpose
Avobenzone 2.7%Sunscreen
Homosalate 4%Sunscreen
Octisalate 4.5%Sunscreen
Octocrylene 6%Sunscreen
Oxybenzone 4.5%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, Silica, Cetyl Dimethicone, Styrene/Acrylates Copolymer, C12-15 Alkyl Benzoate, Steareth-100, Ethylhexylglycerin, Phenoxyethanol, Caprylyl Glycol, Sodium Polyacrylate, Dimethicone, Steareth-2, Polyester-7, Chlorphenesin, Propylene Glycol, Ethylhexyl Stearate, Neopentyl Glycol Diheptanoate, Bisabolol, Disodium EDTA, Butylene Glycol, Acrylates/Dimethicone Copolymer, Diethylhexyl 2,6-Naphthalate, Mannan, Xanthan Gum, BHT, Capryloyl Glycine, Trideceth-6, Sarcosine, Cedrus Atlantica Bark Extract, Cinnamomum Zeylanicum Bark Extract, Portulaca Oleracea Extract

Questions?

Call toll-free 800-582-4048 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 ®
#1 DERMATOLOGIST RECOMMENDED BRAND

Clear Face
BREAKOUT FREE
oil-free
sunscreen
BROAD SPECTRUM SPF 55

55

helioplex ®
broad spectrum uva•uvb

won't cause breakouts
ultra-light

water resistant (80 minutes)

3.0 FL OZ (88 mL)

Principal Display Panel - 88 mL Tube Label
NEUTROGENA CLEAR FACE BREAKOUT FREE OIL FREE BROAD SPECTRUM SPF 55 
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0573
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE27 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE40 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE45 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE60 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE45 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
STEARETH-100 (UNII: 4OH5W9UM87)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
STEARETH-2 (UNII: V56DFE46J5)  
POLYESTER-7 (UNII: 0841698D2F)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
LEVOMENOL (UNII: 24WE03BX2T)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
YEAST MANNAN (UNII: 91R887N59P)  
XANTHAN GUM (UNII: TTV12P4NEE)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)  
TRIDECETH-6 (UNII: 3T5PCR2H0C)  
SARCOSINE (UNII: Z711V88R5F)  
CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF)  
CINNAMON BARK OIL (UNII: XE54U569EC)  
PURSLANE (UNII: M6S840WXG5)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0573-388 mL in 1 TUBE; Type 0: Not a Combination Product10/07/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02010/07/2019
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 10/2023
Document Id: 07e9c65c-52e3-9e0a-e063-6394a90a671d
Set id: 3e25a4ce-dbdd-4830-a3d8-a2dfb3bcb078
Version: 7
Effective Time: 20231017
 
Johnson & Johnson Consumer Inc.