NEUTROGENA MEN TRIPLE PROTECT FACE WITH SUNSCREEN BROAD SPECTRUM SPF 20- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion

Neutrogena Men Triple Protect Face With Sunscreen Broad Spectrum SPF 20 by

Drug Labeling and Warnings

Neutrogena Men Triple Protect Face With Sunscreen Broad Spectrum SPF 20 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 INGREDIENT

Active ingredients	Purpose
Avobenzone 3%	Sunscreen
Homosalate 12%	Sunscreen
Octisalate 5%	Sunscreen
Octocrylene 1.7%	Sunscreen
Oxybenzone 3%	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 and evenly to freshly shaven face and neck every morning.

For Sunscreen Use:

• apply liberally 15 minutes before sun exposure
• reapply: at least every 2 hours
• use a water resistant sunscreen if swimming or sweating
• 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 value of SPF 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, Octyldodecyl Neopentanoate, Glycerin, Glycine Soja (Soybean) Seed Extract, Emulsifying Wax, Glyceryl Stearate, PEG-100 Stearate, Dimethicone, Silica, Phenoxyethanol, Panthenol, Tocopheryl Acetate, Ethylhexylglycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Caprylyl Glycol, Fragrance, Bisabolol, Camellia Sinensis Leaf Extract, Methylparaben, Disodium EDTA, Allantoin, Butylene Glycol, Sodium Hydroxide

Questions?

Call toll-free 866-638-4636 or 215-273-8755 (collect). www.neutrogenamen.com

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

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton

Neutrogena®

MEN

TRIPLE PROTECT
Face Lotion
with
sunscreen

Broad Spectrum
SPF 20

Soothes razor irritation
Relieves dry skin
Helps fight signs of aging

1.7 FL OZ (50mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA MEN TRIPLE PROTECT FACE WITH SUNSCREEN BROAD SPECTRUM SPF 20 
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0520
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	30 mg  in 1 mL
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S)	Homosalate	120 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	50 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	17 mg  in 1 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y)	Oxybenzone	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Octyldodecyl Neopentanoate (UNII: X8725R883T)
Glycerin (UNII: PDC6A3C0OX)
Soybean (UNII: L7HT8F1ZOD)
Glyceryl Monostearate (UNII: 230OU9XXE4)
PEG-100 Stearate (UNII: YD01N1999R)
Dimethicone (UNII: 92RU3N3Y1O)
Silicon Dioxide (UNII: ETJ7Z6XBU4)
Phenoxyethanol (UNII: HIE492ZZ3T)
Panthenol (UNII: WV9CM0O67Z)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Ethylhexylglycerin (UNII: 147D247K3P)
Carbomer Interpolymer Type A (Allyl Sucrose Crosslinked) (UNII: 59TL3WG5CO)
Caprylyl Glycol (UNII: 00YIU5438U)
Levomenol (UNII: 24WE03BX2T)
Green Tea Leaf (UNII: W2ZU1RY8B0)
Methylparaben (UNII: A2I8C7HI9T)
Edetate Disodium Anhydrous (UNII: 8NLQ36F6MM)
Allantoin (UNII: 344S277G0Z)
Butylene Glycol (UNII: 3XUS85K0RA)
Sodium Hydroxide (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0520-1	1 in 1 CARTON	05/17/2019
1		50 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	05/17/2019

Labeler - Johnson & Johnson Consumer Inc. (002347102)