Bellagio Sunscreen For Face SPF 30

Dosage form: lotion
Ingredients: Octinoxate 74.25mg in 1mL, Octocrylene 59.4mg in 1mL, Octisalate 49.5mg in 1mL, Zinc Oxide 29.106mg in 1mL
Labeler: Lifetech Resources, LLC
NDC Code: 65643-325

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

BELLAGIO®
SUNSCREEN
LOTION FOR FACE
SPF 30

DRUG FACTS

ACTIVE INGREDIENTS

Octinoxate 7.50%, Octocrylene 6.00%, Octisalate 5.00%, Zinc Oxide 2.94%

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, Ethylhexyl Isononanoate, Acrylates Copolymer, Butylene Glycol, Cetyl Alcohol, PEG-100 Stearate, Sorbitan Stearate, Polysorbate-60, Glyceryl Stearate, Dimethicone, Squalane, Hydroxylated Lecithin, Xanthan Gum, Allantoin, Tocopheryl Acetate, Centella Asiatica Extract, Echinacea Angustifolia Extract, Vitis Vinifera (Grape) Seed Extract, Citrus Medica Limonum (Lemon) Peel Extract, Melissa Officinalis Extract, Citric Acid, Triethoxycaprylylsilane, Imidazolidinyl Urea, Sodium Benzoate, Disodium EDTA, Potassium Sorbate.

PRINCIPAL DISPLAY PANEL - 118 ML Tube Label

BELLAGIO®
SUNSCREEN
LOTION FOR FACE
SPF 30

4 FL OZ / 118 ML

BELLAGIO SUNSCREEN FOR FACE SPF 30 
octinoxate, octocrylene, octisalate, and zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65643-325
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Octinoxate (Octinoxate) Octinoxate74.25 mg  in 1 mL
Octocrylene (Octocrylene) Octocrylene59.4 mg  in 1 mL
Octisalate (Octisalate) Octisalate49.5 mg  in 1 mL
Zinc Oxide (Zinc Oxide) Zinc Oxide29.106 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Butylene Glycol 
Cetyl Alcohol 
Polyoxyl 100 Stearate 
Sorbitan Monostearate 
Polysorbate 60 
Glyceryl Monostearate 
Dimethicone 
Squalane 
Xanthan Gum 
Allantoin 
.ALPHA.-TOCOPHEROL ACETATE, D- 
CENTELLA ASIATICA 
ECHINACEA ANGUSTIFOLIA 
Lemon Peel 
MELISSA OFFICINALIS 
Citric Acid Monohydrate 
Imidurea 
Sodium Benzoate 
Edetate Disodium 
Potassium Sorbate 
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:65643-325-14118 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35201/01/2009
Labeler - Lifetech Resources, LLC (622559110)
Establishment
NameAddressID/FEIOperations
Lifetech Resources, LLC622559110MANUFACTURE

Revised: 09/2010
 
Lifetech Resources, LLC

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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