Timewise Day Solution sunscreen SPF 35 description, usages, side effects, indications, overdosage, supplying and lots more!

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Timewise Day Solution sunscreen SPF 35

Mary Kay Inc.




FULL PRESCRIBING INFORMATION

Active ingredient


Active Ingredients ; HOMOSALATE (10% w/w) ,OCTISALATE(5% w/w),OXYBENZONE(4%w/w), OCOCRYLENE (2% w/w), AVOBENZONE(2% w/w)



Warnings; For external use only. Not to be swalloed. Avoid contact with the eyes. Discontinue use if signs of irritation or rash appear.



Keep out of reach of children. Do not stay too long in the sun, even while using a sunscreen product.

Uses

Indication; Broad-spectrum UVA/UVB protection.

Water,Dimethicone, Butylene Glycol,Styrene/Acrylates Copolymer,C12-15 Alkyl Benzoate,Dicapryl Carbonate,Glycerin,Ceteareth-25,Dimethicone Crosspolymer,Magnesium Aluminum Silicate, Acetyl Dipeptide-1,Cetyl Ester, Plankton Extract,Hydrolyzed Algin, Adenosin, Pentylene Glycol , Tocopheryl Acetate,Crithmum Marithimum Extract,Ascorbic Acid,Hydrogenated Lecithin,Hydroxyethylcellulose,Dipropylene Glycol,Dibenzoate Acrylate / C12-22 Alkyl Methacrylate Crosspolymer ,Disodium Ethylene Dicocamide PEG-15 Disulfate,Sorbic Acid ,Caprylyl Glycol, PPG-15 Stearyl Ether Benzoate,Propylene Glycol , Xanthan Gum, Cyclopentasiloxane, PEG-75,PEG-150,PEG-6 Cetyl Dimethicone,PEG-4 Laurate,Laureth-3 ,Disodium EDTA , Ammonium Hydroxide,Iodopropyl Butylcarbamate,Methylparaben,Phenoxyethanol

 Timewise Day Solution sunscreen SPF 35

Timewise Day Solution sunscreen SPF 35

Homosalate,Octisalate,Oxybenzone,Octocrylene,Avobenzone CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51531-8363
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OXYBENZONE OXYBENZONE 1.16 mL
AVOBENZONE AVOBENZONE 0.58 mL
OCTISALATE OCTISALATE 1.45 mL
HOMOSALATE Homosalate 2.9 mL
OCTOCRYLENE Octocrylene 0.58 mL

Inactive Ingredients

Ingredient Name Strength
water
BUTYLENE GLYCOL
C12-15 ALKYL BENZOATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51531-8363-0 29 in 1 BOTTLE, DISPENSING

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-03-01


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