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

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Neutrogena Ultra Sheer Dry Touch Sunblock

Neutrogena Corporation

Neutrogena Ultra Sheer Dry-Touch Sunblock SPF 45


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 (USA) or www.neutrogena.com

Active Ingredients

Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 4%, Oxybenzone 5%

Inactive Ingredients

Water
Silica
Styrene/Acrylates Copolymer
Potassium Cetyl Phosphate
Beeswax
Benzyl Alcohol
Glyceryl Stearate
PEG-100 Stearate
Cetyl Dimethicone
Dimethicone
Caprylyl Methicone
Caprylyl Glycol
Ethylhexylglycerin
Behenyl Alcohol
Sodium Polyacrylate
Xanthan Gum
Dimethicone/PEG-10/15 Crosspolymer
Ethylhexyl Stearate
Acrylates/C12-22 Alkyl Methacrylate Copolymer
Disodium EDTA
Chlorphenesin
Fragrance
Diethylhexyl 2,6-Naphthalate
BHT
Trideceth-6

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

PRINCIPAL DISPLAY PANEL - 88 mL Tube Label

Neutrogena ®

Ultra Sheer

DRY-TOUCH
SUNBLOCK

SPF
45

helioplex ®
broad spectrum uva-uvb

LIGHTWEIGHT
CLEAN FEEL

fast absorbing
leaves skin soft and smooth
waterproof

#1 DERMATOLOGIST
RECOMMENDED SUNCARE

3.0 FL OZ (88 mL)

Neutrogena Ultra Sheer Dry Touch Sunblock

Neutrogena Ultra Sheer Dry Touch Sunblock

Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10812-507
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 40 mg
OXYBENZONE OXYBENZONE 50 mg

Inactive Ingredients

Ingredient Name Strength
water
SILICON DIOXIDE
potassium cetyl phosphate
YELLOW WAX
BENZYL ALCOHOL
GLYCERYL MONOSTEARATE
PEG-100 STEARATE
DIMETHICONE
CAPRYLYL GLYCOL
ETHYLHEXYLGLYCERIN
docosanol
XANTHAN GUM
EDETATE DISODIUM
CHLORPHENESIN
Diethylhexyl 2,6-Naphthalate
BUTYLATED HYDROXYTOLUENE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10812-507-01 88 in 1 TUBE
2 14 in 1 TUBE
3 88 in 1 TUBE
4 NDC:10812-507-03 2 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-06-02


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