Diorskin Nude Natural Glow Makeup 010 Ivory description, usages, side effects, indications, overdosage, supplying and lots more!

Diorskin Nude Natural Glow Makeup 010 Ivory

Parfums Christian Dior
Parfums Christian Dior

  • 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
Diorskin Nude Natural Glow Creme Gel Makeup 010



FULL PRESCRIBING INFORMATION

Apply prior to sun exposure.

WARNINGS: For external use only. Keep out of eyes.

Discontinue use if skin irritation develops or increases. If irritation persists, consult a health care practitioner.

Keep out of reach of children.

Active ingredient

ACTIVE INGREDIENTS: OCTINOXATE (ETHYLHEXYL METHOXYCINNAMATE) 3.75 % - OXYBENZONE (BENZOPHENONE-3) 1.00 %.

OTHER INGREDIENTS: ISONONYL ISONONANOATE - CETEARYL ISONONANOATE - DIPHENYL DIMETHICONE/VINYL DIPHENYL DIMETHICONE/SILSESQUIOXANE CROSSPOLYMER - PHENYL TRIMETHICONE - POLYETHYLENE - SILICA - MICA - POLYPROPYLENE - PARAFFIN - OZOKERITE - NYLON-12 - CAPRYLIC/CAPRIC TRIGLYCERIDE - HYDROGENATED POLYCYCLOPENTADIENE - POLYMETHYLSILSESQUIOXANE - SODIUM MYRISTOYL GLUTAMATE - PHENOXYETHANOL - SILICA SILYLATE - TOCOPHERYL ACETATE - PARFUM (FRAGRANCE) - BHT - AQUA (WATER) - LINALOOL - LIMONENE - BUTYLPHENYL METHYLPROPIONAL - CITRONELLOL - ASCORBYL GLUCOSIDE - SERICIN - MAGNESIUM ASPARTATE - ZINC GLUCONATE - RHODOCHROSITE EXTRACT - HYDROLYZED LINSEED EXTRACT - SORBIC ACID - COPPER GLUCONATE.

[+/- : CI 77002 (ALUMINUM HYDROXIDE) - CI 77007 (ULTRAMARINES) - CI 77163 (BISMUTH OXYCHLORIDE) - CI 77491, 77492, 77499 (IRON OXIDES) - CI 77891 (TITANIUM DIOXIDE)]. N 05245/A









































DIORSKIN NUDE

010 IVORY


MADE IN FRANCE



























Diorskin Nude Natural Glow Makeup 010 Ivory

OCTINOXATE, OXYBENZONE PASTE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:61957-2010
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 3.75 g
OXYBENZONE OXYBENZONE 1.00 g

Inactive Ingredients

Ingredient Name Strength
ISONONYL ISONONANOATE
Cetearyl Isononanoate
PHENYL TRIMETHICONE
SILICON DIOXIDE
MICA
PARAFFIN
MEDIUM-CHAIN TRIGLYCERIDES
PHENOXYETHANOL
BUTYLATED HYDROXYTOLUENE
water
LINALOOL, DL-
BUTYLPHENYL METHYLPROPIONAL
.BETA.-CITRONELLOL, R-(+)-
MAGNESIUM ASPARTATE
ZINC GLUCONATE
MANGANESE CARBONATE
sorbic acid
COPPER GLUCONATE
aluminum hydroxide
BISMUTH OXYCHLORIDE
ferric oxide red
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
titanium dioxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 10 in 1 BOTTLE
2 NDC:61957-2010-1 1 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-08-04


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