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Name:Bellagio Sunscreen Spf 30
Manufacturer:Lifetech Resources, Llc
Category:Over-the-counter (OTC) Marketed Drugs


BELLAGIO® SUNSCREEN LOTION SPF 30

BELLAGIO SUNSCREEN SPF 30 - homosalate, octinoxate, octocrylene and oxybenzone lotion 
Lifetech Resources, LLC

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.

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BELLAGIO®
SUNSCREEN
LOTION
SPF 30

DRUG FACTS

ACTIVE INGREDIENTS

Homosalate 10.0%, Octinoxate 7.0 %, Octocrylene 6.5 %, Oxybenzone 5.5 %

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, Cyclopentasiloxane, Cetearyl Alcohol, Ceteareth-20, Polysorbate 60, Butylene Glycol, Potassium Cetyl Phosphate, Stearyl Alcohol, Dimethicone, Sorbitan Stearate, Cetearyl Methicone, Simmondsia Chinensis (Jojoba) Seed Oil, Aloe Barbadensis Leaf Juice, Butyrospermum Parkii (Shea Butter), Tocopheryl Acetate, Calendula Officinalis Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Xanthan Gum, Aminomethyl Propanol, Disodium EDTA, Sodium Benzoate, Potassium Sorbate, Phenoxyethanol, Fragrance.

PRINCIPAL DISPLAY PANEL - 237 ML Tube Label

BELLAGIO®
SUNSCREEN
LOTION
SPF 30

8 FL OZ / 237 ML

Principal Display Panel - 237 ML Tube Label

BELLAGIO SUNSCREEN SPF 30 
homosalate, octinoxate, octocrylene, and oxybenzone lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:65643-334
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Homosalate (Homosalate) Homosalate 100.7 mg  in 1 mL
Octinoxate (Octinoxate) Octinoxate 70.49 mg  in 1 mL
Octocrylene (Octocrylene) Octocrylene 65.455 mg  in 1 mL
Oxybenzone (Oxybenzone) Oxybenzone 55.385 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
Water  
Cyclomethicone 5  
Cetostearyl Alcohol  
POLYOXYL 20 CETOSTEARYL ETHER  
Polysorbate 60  
Butylene Glycol  
Potassium Cetyl Phosphate  
Stearyl Alcohol  
Dimethicone  
Sorbitan Monostearate  
Jojoba Oil  
Aloe Vera Leaf  
Shea Butter  
.ALPHA.-TOCOPHEROL ACETATE, D-  
Calendula Officinalis Flower  
CHAMOMILE  
Xanthan Gum  
Aminomethylpropanol  
Edetate Disodium  
Sodium Benzoate  
Potassium Sorbate  
Phenoxyethanol  
Product Characteristics
Color WHITE Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:65643-334-17 237 mL in 1 TUBE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part352 01/01/2009

Labeler - Lifetech Resources, LLC (622559110)
Establishment
Name Address ID/FEI Operations
Lifetech Resources, LLC 622559110 MANUFACTURE

Revised: 09/2010 Lifetech Resources, LLC



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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