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

Neutrogena Ultra Sheer Dry-Touch Sunblock SPF 70


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Directions

Apply liberally on face and body 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 on 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 15%, Octisalate 5%, Octocrylene 2.8%, Oxybenzone 6%

Inactive Ingredients

Water
Styrene/Acrylates Copolymer
Silica
Diethylhexyl 2,6 - Naphthalate
Beeswax
Caprylyl Methicone
Cetyl Dimethicone
Ethylhexylglycerin
Dipotassium Glycyrrhizate
BHT
Dimethicone
Glyceryl Stearate
PEG-100 Stearate
Sodium Polyacrylate
Acrylates/C12-22 Alkyl Methacrylate Copolymer
Ethylhexyl Stearate
Xanthan Gum
Trideceth-6
Trimethylsiloxysilicate
Disodium EDTA
Polyaminopropyl Biguanide
Methylisothiazolinone
Fragrance

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

PRINCIPAL DISPLAY PANEL - 88 mL Tube Label

Neutrogena®

Ultra Sheer
DRY-TOUCH
SUNBLOCK

SPF
70

with
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:10812-247
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOBENZONE AVOBENZONE 30 mg
HOMOSALATE Homosalate 150 mg
OCTISALATE OCTISALATE 50 mg
OCTOCRYLENE Octocrylene 28 mg
OXYBENZONE OXYBENZONE 60 mg

Inactive Ingredients

Ingredient Name Strength
water
SILICON DIOXIDE
Diethylhexyl 2,6-Naphthalate
YELLOW WAX
ETHYLHEXYLGLYCERIN
GLYCYRRHIZINATE DIPOTASSIUM
BUTYLATED HYDROXYTOLUENE
DIMETHICONE
GLYCERYL MONOSTEARATE
PEG-100 STEARATE
ETHYLHEXYL STEARATE
XANTHAN GUM
TRIDECETH-6
EDETATE DISODIUM
POLYAMINOPROPYL BIGUANIDE
METHYLISOTHIAZOLINONE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10812-247-01 88 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-10-14


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