Mary Kay Tinted Moisturizer Sunscreen SPF 20 Bronze 2 description, usages, side effects, indications, overdosage, supplying and lots more!

Mary Kay Tinted Moisturizer Sunscreen SPF 20 Bronze 2

Mary Kay Inc.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Mary Kay Tinted Moisturizer SPF 20 Bronze 2

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Octinoxate (7.5% W/W)

Octisalate (5% W/W)

Zinc Oxide (2.4% W/W)

Oxybenzone (1.75% W/W)

Warnings

For external use only, not to be swallowed. Avoid contact with the eyes.

Discontinue use

if signs of irritation or rash appear.

Keep out of reach of children.

Indications:

Protects against UVA/UVB rays.

Directions:

Apply prior to sun exposure to clean skin. Reapply as needed.

OTHER INGREDIENTS/AUTRES INGREDIENTS:

WATER/EAU, ISODODECANE, GLYCERIN, PROPYLENE GLYCOL, C12-15 ALKYL BENZOATE, CETEARYL ALCOHOL, BETAINE, GLYCERYL STEARATE, PEG-100 STEARATE, DIMETHICONE PEG-7 PHOSPHATE, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, SQUALANE, HYDROXYETHYLCELLULOSE, METHYLPARABEN, CETEARETH-20, POLYHYDROXYSTEARIC ACID, GLYCERYL POLYACRYLATE, DMDM HYDANTOIN, TOCOPHERYL ACETATE, DISODIUM EDTA, PEG-4 LAURATE, TRIETHOXYCAPRYLYLSILANE, POLYSORBATE-60, BUTYLENE GLYCOL, SORBITAN ISOSTEARATE, IODOPROPYNYL BUTYLCARBAMATE, ALOE BARBADENSIS LEAF EXTRACT, ANTHEMIS NOBILIS FLOWER EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, PHENOXYETHANOL, PROPYLPARABEN, TITANIUM DIOXIDE, IRON OXIDES.

Principal Display Panel - 43 ml carton

Mary Kay

tinted moisturizer with sunscreen spf 20

hydratant teinte avec ecran solaire fps 20

crema humectante con color y fps 20

1.5 FL. OZ. / 43 mL

Principal Display Panel - 43 ml carton

Mary Kay Tinted Moisturizer Sunscreen SPF 20 Bronze 2

octinoxate, octisalate, zinc oxide, oxybenzone, CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51531-7502
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 7.5 g
OCTISALATE OCTISALATE 5 g
Zinc Oxide Zinc oxide 2.4 g
OXYBENZONE OXYBENZONE 1.75 g

Inactive Ingredients

Ingredient Name Strength
water
ISODODECANE
GLYCERIN
propylene glycol
ALKYL (C12-15) BENZOATE
CETOSTEARYL ALCOHOL
BETAINE
GLYCERYL MONOSTEARATE
PEG-100 STEARATE
DIMETHICONE PEG-7 PHOSPHATE
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)
SQUALANE
METHYLPARABEN
POLYOXYL 20 CETOSTEARYL ETHER
POLYHYDROXYSTEARIC ACID (2300 MW)
DMDM HYDANTOIN
.ALPHA.-TOCOPHEROL ACETATE
EDETATE DISODIUM
PEG-4 LAURATE
TRIETHOXYCAPRYLYLSILANE
POLYSORBATE 60
1,3-BUTYLENE GLYCOL
Sorbitan Isostearate
IODOPROPYNYL BUTYLCARBAMATE
Aloe Vera Leaf
CHAMAEMELUM NOBILE FLOWER
GREEN TEA LEAF
PHENOXYETHANOL
PROPYLPARABEN
ferric oxide red
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
titanium dioxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 43 in 1 TUBE
2 NDC:51531-7502-8 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2006-08-16


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