OIL CONTROLLING MAKEUP description, usages, side effects, indications, overdosage, supplying and lots more!

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OIL CONTROLLING MAKEUP

JAFRA COSMETICS INTERNATIONAL

OIL CONTROLLING MAKEUP SPF-15




FULL PRESCRIBING INFORMATION

Active ingredient



Purpose

PURPOSE: SUNSCREEN

OTHER INGREDIENTS: WATER/AQUA, BUTYLENE GLYCOL, ISOPROPYL PALMITATE, ISOPROPYL ISOSTEARATE, POTASSIUM CETHYL PHOSPHATE, HYDROGENATED PALM GLYCERIDES, GLYCERYL STEARATE, DI-PPG-3 MYRISTYL ETHER ADIPATE, SILICA, STEARIC ACID, ZINC OXIDE/CI 77947, POLYSORBATE 20, LECITHIN, POLYSILICONE-11, LAURETH-12, CYCLOPENTASILOXANE, ACRYLATES/DIMETHICONE COPOLYMER, DMDM HYDANTOIN, TRIHYDROXYSTEARIN, MAGNESIUM ALUMINUM SILICATE, XANTHAN GUM, PANTHENOL, IPOMOEA DIGITATA (FINGERLEAF MORNING GLORY) EXTRACT, WITHANIA SOMNIFERIA (WINTER CHERRY) EXTRACT, VIGNA RADIATA (MUNG BEAN) EXTRACT, TOCOPHERYL ACETATE, HAMAMELIS VIRGINIA (WITCH HAZEL) EXTRACT, SYMPHYTUM OFFICINALIS LEAF EXTRACT, CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT, CUCUMIS SATIVAS (CUCUMBER) FRUIT EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, ALTHAEA OFFICINALIS ROOT EXTRACT, MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL, FRAGRANCE/PARFUM, TRISODIUM EDTA, PEG-4 LAURATE, IODOPROPYNYL BUTYLCARBAMATE [MAY CONTAIN, +/-: IRON OXIDES/CI 77491/CI 77492/CI 77499, TITANIUM DIOXIDE/CI 77891]  [FRAGRANCE/PARFUM CONTAINS: LIMONENE, LINALOOL, BUTYLPHENYL METHYLPROPIONAL (LILIAL), CITRONELLOL]

AN OIL FREE, LIQUID MAKEUP THAT CONTROLS EXCESS OIL AND PROVIDES FLAWLESS COVERAGE WITHOUT SHINE.

Uses

SPF 15 PROTECTS AGAINST DAMAGING ULTRAVIOLET RAYS. MATTE FINISH. SHEER TO MEDIUM COVERAGE.

TO USE: SMOOTH ON WITH FINGERS OR SPONGE.

CAUTION: FOR EXTERNAL USE ONLY. AVOID CONTACT WITH EYES.

DISCONTINUE USE IF SIGNS OF IRRITATION OCCUR.

KEEP OUT OF REACH OF CHILDREN.

CLINICALLY, ALLERGY AND IRRITANCY TESTED.

JAFRA

OIL CONTROLLING MAKEUP SPF 15

30 ML / 1 FL OZ

OIL CONTROLLING MAKEUP

OIL CONTROLLING MAKEUP

OCTINOXATE OCTISALATE OXYBENZONE LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68828-046
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 6 g
OCTISALATE OCTISALATE 3 g
OXYBENZONE OXYBENZONE 2 g

Inactive Ingredients

Ingredient Name Strength
water
BUTYLENE GLYCOL
ISOPROPYL PALMITATE
ISOPROPYL ISOSTEARATE
potassium cetyl phosphate
hydrogenated palm glycerides
GLYCERYL MONOSTEARATE
DI-PPG-3 MYRISTYL ETHER ADIPATE
SILICON DIOXIDE
STEARIC ACID
Zinc Oxide
POLYSORBATE 20
LECITHIN, SOYBEAN
Polysilicone-15
LAURETH-12
CYCLOMETHICONE 5
CARBOMER INTERPOLYMER TYPE A (55000 MPA.S)
DMDM HYDANTOIN
TRIHYDROXYSTEARIN
magnesium aluminum silicate
XANTHAN GUM
PANTHENOL
IPOMOEA MAURITIANA TUBER
WITHANIA SOMNIFERA FLOWER
MUNG BEAN
ALPHA-TOCOPHEROL ACETATE
HAMAMELIS VIRGINIANA BARK
COMFREY LEAF
CHAMOMILE
CUCUMBER
Aloe Vera Leaf
ALTHAEA OFFICINALIS ROOT
TEA TREE OIL
EDETATE TRISODIUM
PEG-4 LAURATE
IODOPROPYNYL BUTYLCARBAMATE
ferric oxide red
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
titanium dioxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68828-046-11 30 in 1 BOTTLE
2 NDC:68828-046-67 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-04-19


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