NEUTROGENA CLEAR FACE BREAK OUT FREE SUNSCREEN BROAD SPECTRUM SPF30- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion

Neutrogena Clear Face Break Out Free by

Drug Labeling and Warnings

Neutrogena Clear Face Break Out Free by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredients

Avobenzone 2.5%
Homosalate 5%
Octisalate 4%
Octocrylene 3%
Oxybenzone 4%

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, 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?

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

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Dist. by: JOHNSON & JOHNSON CONSUMER INC., Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 88 mL Tube Label

Neutrogena®

clear face

BREAK-OUT FREE
liquid-lotion

SUNSCREEN
Broad Spectrum SPF 30
30
helioplex®
broad spectrum uva uvb

won't cause break-outs
ultra-light, oil-free
water resistant (80 minutes)

#1 DERMATOLOGIST
RECOMMENDED SUNCARE

3.0 FL OZ (88mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA CLEAR FACE BREAK OUT FREE   SUNSCREEN BROAD SPECTRUM SPF30
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	25 mg  in 1 mL
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S)	Homosalate	50 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	40 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	30 mg  in 1 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y)	Oxybenzone	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)
Levomenol (UNII: 24WE03BX2T)
Butylene Glycol (UNII: 3XUS85K0RA)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Capryloyl Glycine (UNII: 8TY5YO42NJ)
Caprylyl Glycol (UNII: 00YIU5438U)
Cedrus Atlantica Bark (UNII: ITP1Q41UPF)
Chlorphenesin (UNII: I670DAL4SZ)
Cinnamon Bark Oil (UNII: XE54U569EC)
Diethylhexyl 2,6-Naphthalate (UNII: I0DQJ7YGXM)
Dimethicone (UNII: 92RU3N3Y1O)
Edetate Disodium (UNII: 7FLD91C86K)
Ethylhexyl Stearate (UNII: EG3PA2K3K5)
Ethylhexylglycerin (UNII: 147D247K3P)
Yeast Mannan (UNII: 91R887N59P)
Neopentyl Glycol Diheptanoate (UNII: 5LKW3C543X)
Phenoxyethanol (UNII: HIE492ZZ3T)
Polyester-7 (UNII: 0841698D2F)
Purslane (UNII: M6S840WXG5)
Propylene Glycol (UNII: 6DC9Q167V3)
Sarcosine (UNII: Z711V88R5F)
Silicon Dioxide (UNII: ETJ7Z6XBU4)
Steareth-100 (UNII: 4OH5W9UM87)
Steareth-2 (UNII: V56DFE46J5)
Trideceth-6 (UNII: 3T5PCR2H0C)
Xanthan Gum (UNII: TTV12P4NEE)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0010-3	88 mL in 1 TUBE; Type 0: Not a Combination Product	09/01/2011	05/12/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	09/01/2011	05/12/2022

Labeler - Johnson & Johnson Consumer Inc. (002347102)