Neutrogena Pure and Free Baby description, usages, side effects, indications, overdosage, supplying and lots more!

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Neutrogena Pure and Free Baby

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

Neutrogena Pure & Free Baby SunscreenBroad Spectrum SPF 60+


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredients

Titanium Dioxide 4.9%
Zinc Oxide 4.7%

Purpose

Sunscreen

Neutrogena Pure and Free Baby 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 value of 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 age: Ask a doctor

Neutrogena Pure and Free Baby Other information

  • Protect this product from excessive heat and direct sun
  • May stain some fabrics

Inactive Ingredients

Alumina, Arachidyl Alcohol, Arachidyl Glucoside, Ascorbic Acid, Avena Sativa (Oat) Kernel Extract, Beeswax, Behenyl Alcohol, Benzyl Alcohol, BHT, Bisabolol, Butylene Glycol, Butyloctyl Salicylate, Cetyl Dimethicone, Dimethicone, Dimethicone PEG-8 Laurate, Dipotassium Glycyrrhizate, Disodium EDTA, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Hydroxyethyl , Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Methicone, Methylisothiazolinone, Pantothenic Acid, PEG-100 Stearate, PEG-8, Polyaminopropyl Biguanide, Polyhydroxystearic Acid, Polymethyl Methacrylate, Polysorbate 60, Potassium Sorbate, Retinyl Palmitate, Silica, Stearic Acid, Styrene/Acrylates Copolymer, Tocopheryl Acetate, Triethoxycaprylylsilane, Trimethylsiloxysilicate, Trisiloxane, Water, Xanthan Gum

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 - 88 mL Tube Label

Neutrogena®

pure & free®
baby

SUNSCREEN
Broad Spectrum
SPF60+

pureSCREEN®
broad spectrum uva•uvb

naturally sourced
sunscreen ingredients
won't run into eyes and sting
water resistant (80 minutes)

#1 DERMATOLOGIST
RECOMMENDED SUNCARE

3.0 FL OZ (88 mL)

Neutrogena Pure and Free Baby

Neutrogena Pure and Free Baby

Titanium Dioxide and Zinc Oxide LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10812-431
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
titanium dioxide 49 mg
Zinc Oxide Zinc oxide 47 mg

Inactive Ingredients

Ingredient Name Strength
ALUMINUM OXIDE
ARACHIDYL ALCOHOL
ARACHIDYL GLUCOSIDE
ASCORBIC ACID
OAT
YELLOW WAX
docosanol
BUTYLATED HYDROXYTOLUENE
LEVOMENOL
BUTYLENE GLYCOL
BUTYLOCTYL SALICYLATE
DIMETHICONE
DIMETHICONE PEG-8 LAURATE
GLYCYRRHIZINATE DIPOTASSIUM
EDETATE DISODIUM
ETHYLHEXYLGLYCERIN
GLYCERIN
GLYCERYL MONOSTEARATE
Isohexadecane
METHYLISOTHIAZOLINONE
PANTOTHENIC ACID
PEG-100 STEARATE
polyethylene glycol 400
POLYAMINOPROPYL BIGUANIDE
POLYSORBATE 60
POTASSIUM SORBATE
VITAMIN A PALMITATE
SILICON DIOXIDE
STEARIC ACID
.ALPHA.-TOCOPHEROL ACETATE
TRIETHOXYCAPRYLYLSILANE
Trisiloxane
water
XANTHAN GUM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10812-431-01 88 in 1 TUBE
2 NDC:10812-431-05 14 in 1 TUBE
3 NDC:10812-431-02 147 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-10-17


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