Neutrogena Wet Skin Kids Beach and Pool Sunblock description, usages, side effects, indications, overdosage, supplying and lots more!

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Neutrogena Wet Skin Kids Beach and Pool Sunblock

Neutrogena Corporation

Wet Skin Kids Sunblock Stick SPF 70 (Beach & Pool)


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Directions

Ask a doctor before use on children under 6 months of age. Apply liberally and evenly to all exposed areas before sun exposure. Can be applied directly to wet skin. For added protection, reapply after swimming, towel drying, excessive perspiration 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 out of reach of children. If case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately. Package contains small parts, which could cause a choking hazard.

Questions or comments?

1-800-299-4786 (USA) or www.neutrogena.com

Active Ingredients

Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10%, Oxybenzone 10%

Inactive Ingredients

Octyldodecyl Neopentanoate
Neopentyl Glycol Diethylhexanoate
Polyethylene
Paraffin
Ozokerite
C12-15 Alkyl Benzoate
Beeswax
Adipic Acid/Diglycol Crosspolymer
Neopentyl Glycol Diisostearate
Dimethicone
Fragrance
Diethylhexyl 2,6-Naphthalate
BHT

Dist. by Neutrogena Corp.
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 13 g Blister Pack

NEW
Neutrogena®
wet skin
kids
BEACH & POOL

sunblock stick
#1 DETMATOLOGIST RECOMMENDED SUNCARE
SPF 70
helioplex®
broad spectrum uva • uvb

applies on wet
or dry skin
hypoallergenic,
waterproof

NET WT
0.47 OZ (13g)

Neutrogena Wet Skin Kids Beach and Pool Sunblock

Neutrogena Wet Skin Kids Beach and Pool Sunblock

Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone STICK

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10812-972
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 100 mg
OXYBENZONE OXYBENZONE 30 mg

Inactive Ingredients

Ingredient Name Strength
OCTYLDODECYL NEOPENTANOATE
NEOPENTYL GLYCOL DIETHYLHEXANOATE
HIGH DENSITY POLYETHYLENE
PARAFFIN
ALKYL (C12-15) BENZOATE
YELLOW WAX
NEOPENTYL GLYCOL DIISOSTEARATE
DIMETHICONE
Diethylhexyl 2,6-Naphthalate
BUTYLATED HYDROXYTOLUENE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 13 in 1 CARTRIDGE
2 NDC:10812-972-01 1 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-12-05


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