Neutrogena Clear Face Break Out Free description, usages, side effects, indications, overdosage, supplying and lots more!

Neutrogena Clear Face Break Out Free

Neutrogena Corporation
Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Neutrogena Clear Face Break-Out Free Liquid-Lotion Sunscreen Broad Spectrum SPF 30

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

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 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 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

Acrylates/Dimethicone Copolymer, BHT, Bisabolol, Butylene Glycol, C12-15 Alkyl Benzoate, Capryloyl Glycine, Caprylyl Glycol, Cedrus Atlantica Bark Extract, Cetyl Dimethicone, Chlorphenesin, Cinnamomum Zeylanicum Bark Extract, Diethylhexyl 2,6-Naphthalate, Dimethicone, Disodium EDTA, Ethylhexyl Stearate, Ethylhexylglycerin, Mannan, Neopentyl Glycol Diheptanoate Phenoxyethanol, Polyester-7, Portulaca Oleracea Extract, Propylene Glycol, Sarcosine, Silica, Sodium Polyacrylate, Steareth-100, Steareth-2, Styrene/Acrylates Copolymer, Trideceth-6, Xanthan Gum, Water

Questions or comments?

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

Dist. by Neutrogena Corporation, Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 88mL Tube Label

Neutrogena®

clear face

BREAK-OUT FREE
liquid-lotion

SUNSCREEN
Broad Spectrum
SPF 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)

PRINCIPAL DISPLAY PANEL - 88mL Tube Label

Neutrogena Clear Face Break Out Free

Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10812-428
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOBENZONE AVOBENZONE 25 mg
HOMOSALATE Homosalate 50 mg
OCTISALATE OCTISALATE 40 mg
OCTOCRYLENE Octocrylene 30 mg
OXYBENZONE OXYBENZONE 40 mg

Inactive Ingredients

Ingredient Name Strength
BUTYLATED HYDROXYTOLUENE
LEVOMENOL
BUTYLENE GLYCOL
ALKYL (C12-15) BENZOATE
Capryloyl Glycine
CAPRYLYL GLYCOL
CEDRUS ATLANTICA BARK
CHLORPHENESIN
CINNAMON BARK OIL
Diethylhexyl 2,6-Naphthalate
DIMETHICONE
EDETATE DISODIUM
ETHYLHEXYL STEARATE
ETHYLHEXYLGLYCERIN
Yeast Mannan
NEOPENTYL GLYCOL DIHEPTANOATE
PHENOXYETHANOL
Polyester-7
PURSLANE
propylene glycol
Sarcosine
SILICON DIOXIDE
STEARETH-100
STEARETH-2
TRIDECETH-6
XANTHAN GUM
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10812-428-01 88 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-10-19


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