NEUTROGENA NATURALS BRIGHTENING DAILY MOISTURIZER BROAD SPECTRUM SPF 25- titanium dioxide and zinc oxide lotion

Neutrogena naturals Brightening Daily Moisturizer Broad Spectrum SPF 25 by

Drug Labeling and Warnings

Neutrogena naturals Brightening Daily Moisturizer Broad Spectrum SPF 25 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
Titanium Dioxide (4.1%)	Sunscreen
Zinc Oxide (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

For sunscreen use:

• apply generously and evenly 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 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, Caprylic/Capric Triglyceride, Cocoglycerides, Glycerin, Cetearyl Olivate, Caprylyl Methicone, Polyglyceryl-3 Diisostearate, Sorbitan Olivate, Cetearyl Alcohol, Butyrospermum Parkii (Shea) Butter, Heptyl Undecylenate, Aluminum Starch Octenylsuccinate, Gluconolactone, Xanthan Gum, Caprylyl Glycol, Glyceryl Behenate, Aluminum Hydroxide, Stearic Acid, Phenylethyl Resorcinol, Benzyl Alcohol, Ethylhexylglycerin, Cetearyl Glucoside, Sodium Benzoate, Chlorphenesin, 1,2-Hexanediol, Triethoxycaprylylsilane, Fragrance, Citrus Limon (Lemon) Peel Extract, Tropolone, Mica, Titanium Dioxide, Iron Oxides

Questions or comments?

Call toll-free 800-582-4048 or 215-273-8755 (collect). www.neutrogena.com

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

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton

NEW
Neutrogena®
naturals

NO
harsh chemical
sulfates, parabens,
petrolatum, dyes,
phthalates

Brightening
Daily Moisturiser
with
Sunscreen
Broad Spectrum SPF 25

Clinically proven to reduce the
look of skin discoloration for visibly
brighter, more even- toned skin

With skin-brightening lemon peel
bionutrients and 100 % naturally
derived sunscreens

Lightweight, won't clog pores
94% naturally derived.
1.7 FL OZ (50 mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA NATURALS BRIGHTENING DAILY MOISTURIZER BROAD SPECTRUM SPF 25 
titanium dioxide and zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0019
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Titanium Dioxide (UNII: 15FIX9V2JP) (Titanium Dioxide - UNII:15FIX9V2JP)	Titanium Dioxide	41 mg  in 1 mL
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z)	Zinc Oxide	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Medium-Chain Triglycerides (UNII: C9H2L21V7U)
Coco-Glycerides (UNII: ISE9I7DNUG)
Glycerin (UNII: PDC6A3C0OX)
Cetearyl Olivate (UNII: 58B69Q84JO)
Caprylyl Trisiloxane (UNII: Q95M2P1KJL)
Polyglyceryl-3 Diisostearate (UNII: 46P231IQV8)
Sorbitan Olivate (UNII: MDL271E3GR)
Cetostearyl Alcohol (UNII: 2DMT128M1S)
Shea Butter (UNII: K49155WL9Y)
Heptyl Undecylenate (UNII: W77QUB6GXO)
Aluminum Starch Octenylsuccinate (UNII: I9PJ0O6294)
Gluconolactone (UNII: WQ29KQ9POT)
Xanthan Gum (UNII: TTV12P4NEE)
Stearic Acid (UNII: 4ELV7Z65AP)
Caprylyl Glycol (UNII: 00YIU5438U)
Glyceryl Dibehenate (UNII: R8WTH25YS2)
Aluminum Hydroxide (UNII: 5QB0T2IUN0)
Phenylethyl Resorcinol (UNII: G37UFG162O)
Cetearyl Glucoside (UNII: 09FUA47KNA)
Sodium Benzoate (UNII: OJ245FE5EU)
Ethylhexylglycerin (UNII: 147D247K3P)
Benzyl Alcohol (UNII: LKG8494WBH)
Lemon Peel (UNII: 72O054U628)
Tropolone (UNII: 7L6DL16P1T)
Mica (UNII: V8A1AW0880)
Chlorphenesin (UNII: I670DAL4SZ)
1,2-Hexanediol (UNII: TR046Y3K1G)
Ferric Oxide Red (UNII: 1K09F3G675)
Triethoxycaprylylsilane (UNII: LDC331P08E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0019-1	1 in 1 CARTON	06/01/2016
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	06/01/2016

Labeler - Johnson & Johnson Consumer Inc. (002347102)