Bellagio Sunscreen SPF 45 description, usages, side effects, indications, overdosage, supplying and lots more!

Bellagio Sunscreen SPF 45

Lifetech Resources, LLC

  • 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
BELLAGIO SUNSCREEN LOTION SPF 45

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

DRUG FACTS

ACTIVE INGREDIENTS

Homosalate 14.00%, Octinoxate 6.50%, Octisalate 5.00%, Oxybenzone 5.00%, Zinc Oxide 2.74%

PURPOSE

Sunscreen

USE

Helps prevent sunburn. Higher SPF gives more sunburn protection.

DIRECTIONS FOR USE

Apply evenly and liberally to all exposed areas before sun exposure. Ensure complete coverage. Reapply as needed or after swimming, towel drying, perspiring, or vigorous activity. Ask a doctor before use on children under 6 months of age.

WARNING

For external use only.

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash or irritation develops and lasts.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENTS

Water, Acrylates Copolymer, Caprylic/Capric Triglyceride, Cyclopentasiloxane, Polysorbate 60, Polysorbate 20, Glycerin, Cetearyl Alcohol, Ceteareth-20, Sorbitan Stearate, Potassium Cetyl Phosphate, Dimethicone, Butyrospermum Parkii (Shea Butter), Squalane, Sodium PCA, Panthenol, Tocopheryl Acetate, Xanthan Gum, Triethoxycaprylylsilane, Disodium EDTA, Sodium Benzoate, Potassium Sorbate, Imidazolidinyl Urea.

PRINCIPAL DISPLAY PANEL - 237 ML Tube Label

BELLAGIO ®
SUNSCREEN
LOTION
SPF 45

8 FL OZ / 237 ML

PRINCIPAL DISPLAY PANEL - 237 ML Tube Label

Bellagio Sunscreen SPF 45

Homosalate, Octinoxate, Octisalate, Oxybenzone, and Zinc Oxide LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:65643-335
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HOMOSALATE Homosalate 143.22 mg
OCTINOXATE OCTINOXATE 66.495 mg
OCTISALATE OCTISALATE 51.15 mg
OXYBENZONE OXYBENZONE 51.15 mg
Zinc Oxide Zinc oxide 28.03 mg

Inactive Ingredients

Ingredient Name Strength
water
MEDIUM-CHAIN TRIGLYCERIDES
CYCLOMETHICONE 5
POLYSORBATE 60
CETOSTEARYL ALCOHOL
POLYOXYL 20 CETOSTEARYL ETHER
POLYSORBATE 20
SORBITAN MONOSTEARATE
potassium cetyl phosphate
DIMETHICONE
SHEA BUTTER
SQUALANE
SODIUM PYRROLIDONE CARBOXYLATE
PANTHENOL
.ALPHA.-TOCOPHEROL ACETATE, D-
XANTHAN GUM
EDETATE DISODIUM
SODIUM BENZOATE
POTASSIUM SORBATE
IMIDUREA
Octyltriethoxysilane

Product Characteristics

Color
WHITE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:65643-335-18 237 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2009-01-01


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