TIMEWISE DAY SOLUTION SUNSCREEN SPF 35- homosalate,octisalate,oxybenzone,octocrylene,avobenzone cream

Timewise Day Solution sunscreen SPF 35 by

Drug Labeling and Warnings

Timewise Day Solution sunscreen SPF 35 by is a Otc medication manufactured, distributed, or labeled by Mary Kay Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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

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

INDICATIONS & USAGE

Indication; Broad-spectrum UVA/UVB protection.

INACTIVE INGREDIENT

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

PRINCIPAL DISPLAY PANEL

 

INGREDIENTS AND APPEARANCE

TIMEWISE DAY SOLUTION SUNSCREEN SPF 35 
homosalate,octisalate,oxybenzone,octocrylene,avobenzone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51531-8363
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y)	Oxybenzone	1.16 mL  in 29 mL
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	0.58 mL  in 29 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	1.45 mL  in 29 mL
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S)	Homosalate	2.9 mL  in 29 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	0.58 mL  in 29 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
C12-15 Alkyl Benzoate (UNII: A9EJ3J61HQ)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	03/01/2012

Labeler - Mary Kay Inc. (103978839)