Rendrevie Sun Screen SPF35 PA description, usages, side effects, indications, overdosage, supplying and lots more!

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Rendrevie Sun Screen SPF35 PA

Cellinbio Co Ltd
Cellinbio Co Ltd

Rendrevie Sun Screen SPF35 PA++


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Octinoxate 7.50%
Titanium Dioxide 5.19%
Octisalate 3.00%

Purpose

Sunscreen

Keep out of Reach of Children

Keep out of reach of children
If swallowed, get medical help or contact a Posion Control Center right away.

Indication & Usage


Directions




Warnings

Warnings

Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not skin cancer or early skin aging

For extenal 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.

Dosage & Administration

Helps prevent sunburn

Inactive Ingredient

Water, Cyclopentasiloxane, Glycerin, Dipropylene Glycol, Peg-10 Dimethicone, Hexyl Laurate, Talc, Dimethicone, Dimethicone/Vinyl Dimethicone Crosspolymer, Disteardimonium Hectorite, Magnesium Sulfate, Aluminum Hydroxide, Aluminum Stearate, Fragrance, Imidazolidinyl Urea, Methylparaben, Propylparaben, Aloe Barbadensis Leaf Juice, Chamomilla Recutita(Matricaria) Flower Extract, Lavandula Angustifolia(Lavender) Extract, Panax Ginseng Root Extract, Squalane, Iron Oxides(CI 77492, CI 77491, CI 77499), Butylparaben, Methicone

Rendrevie Sun Screen SPF35 PA++

NRC Rendrevie sun sunscreen SPF35 PA++

Net WT. 2.54FL OZ(75ml)

Rendrevie Sun Screen SPF35 PA

Rendrevie Sun Screen SPF35 PA

OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:76173-1001
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 5.625 mL
titanium dioxide 3.89 mL
OCTISALATE OCTISALATE 2.25 mL

Inactive Ingredients

Ingredient Name Strength
water
CYCLOMETHICONE 5
GLYCERIN
DIPROPYLENE GLYCOL
HEXYL LAURATE
talc
DIMETHICONE
DISTEARYLDIMONIUM CHLORIDE
MAGNESIUM SULFATE ANHYDROUS
algeldrate
aluminum stearate
IMIDUREA
METHYLPARABEN
PROPYLPARABEN
Aloe Vera Leaf
CHAMOMILE
LAVANDULA ANGUSTIFOLIA FLOWER
ASIAN GINSENG
SQUALANE
FERRIC OXIDE YELLOW
BUTYLPARABEN
ferric oxide red
FERROSOFERRIC OXIDE

Product Characteristics

Color
white (black, red and silver)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:76173-1001-1 75 in 1 TUBE
2 NDC:76173-1001-2 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-07-20


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