UV LOCK ULTRA PACT SUN description, usages, side effects, indications, overdosage, supplying and lots more!

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UV LOCK ULTRA PACT SUN

NATURE REPUBLIC CO., LTD.
NATURE REPUBLIC CO., LTD.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

Active Ingredients: TITANIUM DIOXIDE 7.7%, ETHYLHEXYL METHOXYCINNAMATE 3%, ZINC OXIDE 2.9%

INACTIVE INGREDIENT

Inactive Ingredients:
MICA, TALC, SILICA, DIMETHICONE, NYLON-12, BISMUTH OXYCHLORIDE, MAGNESIUM STEARATE, TRIETHOXYCAPRYLYLSILANE, PHENYL METHICONE, CAPRYLIC/CAPRIC TRIGLYCERIDE, LAUROYL LYSINE, SQUALANE, DIPHENYL DIMETHICONE/VINYL DIPHENYL DIMETHICONE/SILSESQUIOXANE CROSSPOLYMER, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, DIISOSTEARYL MALATE, LANOLIN WAX, IRON OXIDES, ALUMINUM MYRISTATE, FRAGRANCE, METHICONE, METHYLPARABEN, ALLANTOIN, TOCOPHERYL ACETATE, OPUNTIA FICUS-INDICA EXTRACT, PORTULACA OLERACEA EXTRACT, ARNICA MONTANA FLOWER EXTRACT, CENTAUREA CYANUS FLOWER EXTRACT, DIANTHUS CARYOPHYLLUS FLOWER EXTRACT, FREESIA REFRACTA EXTRACT, IRIS VERSICOLOR EXTRACT, JASMINUM OFFICINALE (JASMINE) FLOWER/LEAF EXTRACT, ZANTEDESCHIA AETHIOPICA FLOWER/STEM EXTRACT, C9-15 FLUOROALCOHOL PHOSPHATE, PROPYLPARABEN, WATER, BUTYLENE GLYCOL

PURPOSE

Purpose: Pact type sun block for UV ray protection, especially effective for touchup.

WARNINGS

Cautions:
For external use only.
Avoid contact with eyes and mouth.
Discontinue use if signs of irritation or rash appear.
Keep out of reach of children.
Replace the cap after use.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

UV LOCK ULTRA PACT SUN DOSAGE AND ADMINISTRATION

How to Use:
Turn the cap a little to open, and hold the upper cover with the puff.
Dispense an appropriate amount on the puff, and apply it to the entire face with a tapping motion.

UV LOCK ULTRA PACT SUN INDICATIONS AND USAGE

How to Use:
Turn the cap a little to open, and hold the upper cover with the puff.
Dispense an appropriate amount on the puff, and apply it to the entire face with a tapping motion.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

UV LOCK ULTRA PACT SUN

UV LOCK ULTRA PACT SUN

TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51346-041
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
titanium dioxide 0.62 g
OCTINOXATE OCTINOXATE 0.24 g
Zinc Oxide Zinc oxide 0.23 g

Inactive Ingredients

Ingredient Name Strength
MICA
talc
SILICON DIOXIDE
DIMETHICONE
BISMUTH OXYCHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51346-041-01 8 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-01-02


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