NEUTROGENA DEEP MOISTURE DAY WITH SUNSCREEN BROAD SPECTRUM SPF20- avobenzone, homosalate, octisalate, and octocrylene cream

Neutrogena Deep Moisture Day by

Drug Labeling and Warnings

Neutrogena Deep Moisture Day 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 (2%)	Sunscreen
Homosalate (4%)	Sunscreen
Octisalate (4%)	Sunscreen
Octocrylene (2%)	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 evenly over face and neck every morning after cleansing.

For sunscreen use:

• apply liberally 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, glycerin, dimethicone, isononyl isononanoate, ethylhexyl palmitate, steareth-2, butyrospermum parkii (shea) butter, styrene/acrylates copolymer, silica, steareth-21, methyl methacrylate crosspolymer, BHT, ascorbyl glucoside, tocopheryl acetate, behenyl alcohol, dimethicone crosspolymer, xylitylglucoside, mica, titanium dioxide, ammonium acryloyldimethyltaurate/VP copolymer, sclerotium gum, calcium chloride, cholecalciferol, caprylic/capric triglyceride, disodium EDTA, caprylyl glycol, phenoxyethanol, propylparaben, ehylparaben, methylparaben, citric acid, sodium hydroxide, fragrance

Questions?

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

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

PRINCIPAL DISPLAY PANEL - 63 g Jar Carton

deep moisture
day cream
with
sunscreen

Broad Spectrum SPF20

Intensely moisturizes without a heavy, greasy feel

Neutrogena®

DERMATOLOGIST RECOMMENDED

NET WT 2.25 OZ (63g)

INGREDIENTS AND APPEARANCE

NEUTROGENA DEEP MOISTURE DAY   WITH SUNSCREEN BROAD SPECTRUM SPF20
avobenzone, homosalate, octisalate, and octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0133
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	20 mg  in 1 g
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S)	Homosalate	40 mg  in 1 g
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	40 mg  in 1 g
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	20 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
Dimethicone (UNII: 92RU3N3Y1O)
Isononyl Isononanoate (UNII: S4V5BS6GCX)
Ethylhexyl Palmitate (UNII: 2865993309)
Steareth-2 (UNII: V56DFE46J5)
Shea Butter (UNII: K49155WL9Y)
Silicon Dioxide (UNII: ETJ7Z6XBU4)
Steareth-21 (UNII: 53J3F32P58)
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)
Ascorbyl Glucoside (UNII: 2V52R0NHXW)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Docosanol (UNII: 9G1OE216XY)
Dimethicone Crosspolymer (450000 Mpa.S at 12% in Cyclopentasiloxane) (UNII: UF7620L1W6)
Xylitylglucoside (UNII: O0IEZ166FB)
Mica (UNII: V8A1AW0880)
Titanium Dioxide (UNII: 15FIX9V2JP)
Ammonium Acryloyldimethyltaurate/VP Copolymer (UNII: W59H9296ZG)
Betasizofiran (UNII: 2X51AD1X3T)
Calcium Chloride (UNII: M4I0D6VV5M)
Cholecalciferol (UNII: 1C6V77QF41)
Medium-Chain Triglycerides (UNII: C9H2L21V7U)
Edetate Disodium (UNII: 7FLD91C86K)
Caprylyl Glycol (UNII: 00YIU5438U)
Phenoxyethanol (UNII: HIE492ZZ3T)
Propylparaben (UNII: Z8IX2SC1OH)
Ethylparaben (UNII: 14255EXE39)
Methylparaben (UNII: A2I8C7HI9T)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Sodium Hydroxide (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0133-2	1 in 1 CARTON	05/01/2013
1		63 g in 1 JAR; 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	05/01/2013

Labeler - Johnson & Johnson Consumer Inc. (002347102)