Neutrogena Ultra Sheer Dry Touch description, usages, side effects, indications, overdosage, supplying and lots more!

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Neutrogena Ultra Sheer Dry Touch

Neutrogena Corporation

Neutrogena Ultra Sheer Dry-Touch Sunblock SPF 55


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Directions

Apply liberally and evenly to all exposed areas 15-30 minutes before sun exposure. For added protection, reapply after swimming, towel drying, or extended sun exposure.

Warnings

For external use only.

Not to be swallowed. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

Discontinue use if irritation or rash appear.

Use of children under 6 months of age only with advice of a physician.

Keep this and all drugs out of the reach of children. If case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Questions or comments?

1-800-299-4786 or www.neutrogena.com

Active Ingredients

Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 2.8%, Oxybenzone 6%

Inactive Ingredients

Water
Butyloctyl Salicylate
Styrene/Acrylates Copolymer
Silica
Diethylhexyl 2,6-Naphthalate
VP/Hexadecene Copolymer
Dimethicone
Ethylhexylglycerin
Caprylyl Methicone
Phenoxyethanol
Ethylhexyl Stearate
BHT
Glyceryl Stearate
PEG-100 Stearate
Trideceth-6
Behenyl Alcohol
Trimethylsiloxysilicate
Sodium Polyacrylate
Xanthan Gum
Disodium EDTA
Methylparaben
Iodopropynyl Butylcarbamate
Propylparaben
Ethylparaben
Fragrance

© Dist. by Neutrogena Corp.,
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 88 mL Tube Label

EDITORS
allure
AWARD CHOICE

Neutrogena®

Ultra Sheer
DRY-TOUCH
SUNBLOCK

SPF
55
with
helioplex
broad spectrum uva-uvb®

non-greasy
leaves skin soft and smooth
waterproof

#1 DERMATOLOGIST
RECOMMENDED SUNCARE

3.0 FL OZ (88 mL)

Neutrogena Ultra Sheer Dry Touch

Neutrogena Ultra Sheer Dry Touch

Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10812-193
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOBENZONE AVOBENZONE 30 mg
HOMOSALATE Homosalate 100 mg
OCTISALATE OCTISALATE 50 mg
OCTOCRYLENE Octocrylene 28 mg
OXYBENZONE OXYBENZONE 60 mg

Inactive Ingredients

Ingredient Name Strength
water
BUTYLOCTYL SALICYLATE
SILICON DIOXIDE
Diethylhexyl 2,6-Naphthalate
DIMETHICONE
ETHYLHEXYLGLYCERIN
MYRISTYL TRISILOXANE
PHENOXYETHANOL
ETHYLHEXYL STEARATE
BUTYLATED HYDROXYTOLUENE
GLYCERYL MONOSTEARATE
PEG-100 STEARATE
TRIDECETH-6
docosanol
XANTHAN GUM
EDETATE DISODIUM
METHYLPARABEN
IODOPROPYNYL BUTYLCARBAMATE
PROPYLPARABEN
ETHYLPARABEN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10812-193-01 88 in 1 TUBE
2 14 in 1 TUBE
3 NDC:10812-193-02 29 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-03-12


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