Tinted Moisturizer SPF20 description, usages, side effects, indications, overdosage, supplying and lots more!

Tinted Moisturizer SPF20

CBI Laboratories, 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
skin-perfecting tinted moisturizer SPF 20 SUNCARE ESSENTIALS dark

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purpose
Octinoxate 5% sunscreen
Titanium Dioxide 4.2% sunscreen

Uses

  • provides moderate sun protection

Warnings

  • for external use only
  • for adult use only

When using this product

  • keep out of eyes. If contact occurs rinse with water to remove.
  • Stop use if irritation occurs.
  • Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

Directions

  • Apply liberally 20 minutes before sun exposure and reapply as needed.
  • Children under 6 months of age: ask a physician.

Inactive ingredients

Aluminum Hydroxide, Aluminum Starch Octenylsuccinate, C12-15 Alkyl Benzoate, Cetyl Dimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Chlorphenesin, Cyclopentasiloxane, Disodium EDTA, Ethylhexyl Stearate, Hexyl Laurate, Hydrogenated Castor Wax, Iron Oxides (CI 77492,77491, 77499), Magnesium Sulfate, Microcrystalline Wax, Polyglyceryl-4 Diisostearate, Polyglyceryl-4 Isostearate, Polyhydroxystearate Sebacate, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Stearic Acid, Titanium Dioxide (CI 77891), Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Water (Aqua)

PRINCIPAL DISPLAY PANEL - 48.2 g Carton

skin-perfecting
tinted moisturizer

SPF 20

SUNCARE
ESSENTIALS

dark

Net Wt. 1.7 Oz / 48.2 g

PRINCIPAL DISPLAY PANEL - 48.2 g Carton

Tinted Moisturizer SPF20

OCTINOXATE and TITANIUM DIOXIDE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:24623-049
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.05 g
titanium dioxide 0.042 g

Inactive Ingredients

Ingredient Name Strength
POLYGLYCERYL-4 ISOSTEARATE
ETHYLHEXYL STEARATE
water
cyclomethicone
C12-15 ALKYL BENZOATE
HYDROGENATED CASTOR OIL
MICROCRYSTALLINE WAX
ferric oxide red
FERROSOFERRIC OXIDE
FERRIC OXIDE YELLOW
CHLORPHENESIN
MAGNESIUM SULFATE, UNSPECIFIED
EDETATE DISODIUM
STEARIC ACID

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:24623-049-17 48.2 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2007-04-01


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