CALIFORNIA ALOE OIL FREE SUN BLOCK description, usages, side effects, indications, overdosage, supplying and lots more!

CALIFORNIA ALOE OIL FREE SUN BLOCK

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

  • 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

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

Active Ingredients: ETHYLHEXYL METHOXYCINNAMATE 6.00%, ETHYLHEXYL SALICYLATE 3.00%

INACTIVE INGREDIENT

Ingredients:
WATER, BUTYLENE GLYCOL, CYCLOPENTASILOXANE, ALCOHOL, ISOAMYL P-METHOXYCINNAMATE, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, 1,2-HEXANEDIOL, DIPROPYLENE GLYCOL, PEG/PPG-30/10 DIMETHICONE, TRIETHANOLAMINE, WATER, BUTYLENE GLYCOL, ALOE BARBADENSIS LEAF EXTRACT, 1,2-HEXANEDIOL, PENTYLENE GLYCOL, CAPRYLYL GLYCOL, FRAGRANCE, SILICA, CARBOMER, CETETH-10, PHENOXYETHANOL, ALLANTOIN, BEHENYL ALCOHOL, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, SEA WATER, BUTYLENE GLYCOL, WATER, PHENOXYETHANOL, MORINDA CITRIFOLIA EXTRACT, ETHYLHEXYLGLYCERIN, WATER, BUTYLENE GLYCOL, HIBISCUS ROSA-SINENSIS FLOWER/LEAF EXTRACT, PHENOXYETHANOL, TOCOPHERYL ACETATE, SODIUM HYALURONATE

PURPOSE

Purpose: UV Protection

WARNINGS

Cautions:
For external use only.
Discontinue use if signs of irritation or rashes appear.
Keep out of reach of children.
Replace the cap after use.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE


How to Use: Take an adequate amount of the product and thoroughly apply on the areas exposed to the UV rays

DOSAGE AND ADMINISTRATION


How to Use: Take an adequate amount of the product and thoroughly apply on the areas exposed to the UV rays

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CALIFORNIA ALOE OIL FREE SUN BLOCK

OCTINOXATE, OCTISALATE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51346-243
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 4.8 mg
OCTISALATE OCTISALATE 2.4 mg

Inactive Ingredients

Ingredient Name Strength
water
BUTYLENE GLYCOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51346-243-01 80 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2014-02-01


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Be sure to consult your doctor before taking any medication!
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