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Product NDC Code | 50090-6558 | ||||||||
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Drug Name | Neutrogena ultra sheer dry touch sunscreen broad spectrum spf45 |
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Type | Brand | ||||||||
Active Ingredients |
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Route | TOPICAL | ||||||||
Dosage Form | LOTION | ||||||||
Application Number | M020 | ||||||||
Labeler Name | A-S Medication Solutions | ||||||||
Packages |
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Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Active ingredients Purpose Avobenzone 3% Sunscreen Homosalate 10% Sunscreen Octisalate 5% Sunscreen Octocrylene 10% Sunscreen
Avobenzone 3% | Sunscreen |
Homosalate 10% | Sunscreen |
Octisalate 5% | Sunscreen |
Octocrylene 10% | Sunscreen |
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.Directions apply liberally 15 minutes before sun exposure reapply: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m. - 2 p.m. wear long-sleeved shirts, pants, hats and sunglasses Children under 6 months of age: Ask a doctor
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients Water, Styrene/Acrylates Copolymer, Silica, Dimethicone, Potassium Cetyl Phosphate, Benzyl Alcohol, Beeswax, Caprylyl Methicone, Glyceryl Stearate, PEG-100 Stearate, Cetyl Dimethicone, Caprylyl Glycol, Ethylhexylglycerin, Aluminum Starch Octenylsuccinate, Behenyl Alcohol, Acrylates/Dimethicone Copolymer, Xanthan Gum, Sodium Polyacrylate, Chlorphenesin, Dimethicone PEG - 10/15 Crosspolymer, Hydrolyzed Jojoba Esters, Fragrance, Disodium EDTA, Ethylhexyl Stearate, Tocopheryl Acetate, BHT, Trideceth-6, Jojoba Esters
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.Uses helps prevent sunburn if used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun
Purpose
Information about the drug product’s indications for use.Active ingredients Purpose Avobenzone 3% Sunscreen Homosalate 10% Sunscreen Octisalate 5% Sunscreen Octocrylene 10% Sunscreen
Avobenzone 3% | Sunscreen |
Homosalate 10% | Sunscreen |
Octisalate 5% | Sunscreen |
Octocrylene 10% | Sunscreen |
Spl product data elements
Usually a list of ingredients in a drug product.Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF45 Avobenzone, Homosalate, Octisalate, and Octocrylene BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER SILICON DIOXIDE DIMETHICONE POTASSIUM CETYL PHOSPHATE BENZYL ALCOHOL YELLOW WAX CAPRYLYL TRISILOXANE GLYCERYL MONOSTEARATE PEG-100 STEARATE CAPRYLYL GLYCOL ETHYLHEXYLGLYCERIN ALUMINUM STARCH OCTENYLSUCCINATE DOCOSANOL XANTHAN GUM CHLORPHENESIN HYDROLYZED JOJOBA ESTERS (ACID FORM) EDETATE DISODIUM ANHYDROUS ETHYLHEXYL STEARATE .ALPHA.-TOCOPHEROL ACETATE BUTYLATED HYDROXYTOLUENE TRIDECETH-6 JOJOBA OIL, RANDOMIZED AVOBENZONE AVOBENZONE HOMOSALATE HOMOSALATE OCTISALATE OCTISALATE OCTOCRYLENE OCTOCRYLENE CETYL DIMETHICONE 25 DIMETHICONE/PEG-10/15 CROSSPOLYMER WATER
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.avobenzone, homosalate, octisalate, and octocrylene lotion Label Image
Spl unclassified section
Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.Drug Facts
Distributed by: JOHNSON & JOHNSON CONSUMER INC. Skillman, NJ 08558
Do not use
Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.Do not use on damaged or broken skin
Keep out of reach of children
Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away
Questions
A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.Questions? Call toll-free 800-299-4786 or 215-273-8755 (collect). www.neutrogena.com
Stop use
Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.Stop use and ask a doctor if rash occurs
When using
Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.When using this product keep out of eyes. Rinse with water to remove.
How supplied
Information about the available dosage forms to which the labeling applies, and for which the manufacturer or distributor is responsible. This field ordinarily includes the strength of the dosage form (in metric units), the units in which the dosage form is available for prescribing, appropriate information to facilitate identification of the dosage forms (such as shape, color, coating, scoring, and National Drug Code), and special handling and storage condition information.HOW SUPPLIED Product: 50090-6558 NDC: 50090-6558-0 88 mL in a TUBE / 12 in a CARTON
Storage and handling
Information about safe storage and handling of the drug product.Other information protect this product from excessive heat and direct sun may stain some fabrics
Warnings
Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.Warnings For external use only Do not use on damaged or broken skin When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API