NEUTROGENA SPECTRUM PLUS FACE ADVANCED OIL FREE SUNSCREEN BROAD SPECTRUM SPF100 PLUS- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion

Neutrogena Spectrum Plus Face Advanced Oil Free by

Drug Labeling and Warnings

Neutrogena Spectrum Plus Face Advanced Oil Free by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc., Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredients

Avobenzone 3%
Homosalate 15%
Octisalate 5%
Octocrylene 10%
Oxybenzone 6%

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 generously 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 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: Ask a doctor

Other information

• Protect this product from excessive heat and direct sun

Inactive Ingredients

Water, Styrene/Acrylates Copolymer, Silica, Beeswax, Glycine Soja (Soybean) Seed Extract, Cyclopentasiloxane, Glyceryl Stearate, PEG-100 Stearate, Ethylhexylglycerin, Acrylates/Dimethicone Copolymer, Tocopherol, Caprylyl Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Chlorphenesin, Triethanolamine, Disodium EDTA, Dipotassium Glycyrrhizate, BHT, Chrysanthemum Parthenium (Feverfew) Leaf/Flower/Stem Juice, Methylisothiazolinone, Diethylhexyl 2,6-Naphthalate

Questions

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

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Dist. by Neutrogena Corporation
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 73mL Tube Carton

Neutrogena®

spectrum+
face

ADVANCED
oil-free lotion

SUNSCREEN
Broad Spectrum
SPF 100+

Helioplex 360°
Full spectrum uva uvb

advanced antioxidant complex
won't clog pores or cause
breakouts
water resistant (80 minutes)

RECOMMENDED
Skin
Cancer
Foundation
RECOMMENDED
AS AN EFFECTIVE
UV SUNSCREEN

#1 DERMATOLOGIST
RECOMMENDED SUNCARE

2.5 FL OZ (73mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA SPECTRUM PLUS FACE ADVANCED OIL FREE   SUNSCREEN BROAD SPECTRUM SPF100 PLUS
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10812-042
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	150 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	50 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	100 mg  in 1 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y)	Oxybenzone	60 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Silicon Dioxide (UNII: ETJ7Z6XBU4)
Yellow Wax (UNII: 2ZA36H0S2V)
Soybean (UNII: L7HT8F1ZOD)
Cyclomethicone 5 (UNII: 0THT5PCI0R)
Glyceryl Monostearate (UNII: 230OU9XXE4)
PEG-100 Stearate (UNII: YD01N1999R)
Ethylhexylglycerin (UNII: 147D247K3P)
Tocopherol (UNII: R0ZB2556P8)
Caprylyl Glycol (UNII: 00YIU5438U)
Chlorphenesin (UNII: I670DAL4SZ)
Trolamine (UNII: 9O3K93S3TK)
Edetate Disodium (UNII: 7FLD91C86K)
Glycyrrhizinate Dipotassium (UNII: CA2Y0FE3FX)
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)
Feverfew (UNII: Z64FK7P217)
Methylisothiazolinone (UNII: 229D0E1QFA)
Diethylhexyl 2,6-Naphthalate (UNII: I0DQJ7YGXM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10812-042-01	1 in 1 CARTON	10/22/2012	12/01/2023
1		73 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	10/22/2012	12/01/2023

Labeler - Johnson & Johnson Consumer Inc. (002347102)

Registrant - Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. (830803164)