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Intensite creme lustre day spf 30 us - Medication Information

Product NDC Code 82691-142
Drug Name

Intensite creme lustre day spf 30 us

Type Brand
Active Ingredients
Avobenzone 30 mg/ml
Octisalate 50 mg/ml
Octocrylene 80 mg/ml
Route TOPICAL
Dosage Form CREAM
Application Number M020
Labeler Name RV Skincare LLC
Packages
Package NDC Code Description
82691-142-00 1 jar in 1 carton (82691-142-00) / 50 ml in 1 jar
82691-142-01 5 ml in 1 jar (82691-142-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredients Avobenzone 3.0% Octisalate 5.0% Octocrylene 8.0% Purpose 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 • For sunscreen use: • apply liberally 15 minutes before sun exposure • use a water resistant sunscreen if swimming or sweating • reapply at least every 2 hours • 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 Sun Protection Measures.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients: Aqua (Water, Eau), Helianthus Annuus (Sunflower) Seed Oil, Cyclopentasiloxane, Undecylcrylene Dimethicone, Butyloctyl Salicylate, Butylene Glycol, Cetearyl Alcohol, C13-15 Alkane, Glycerin, Sorbitan Stearate, PPG-2 Myristyl Ether Propionate, Potassium Cetyl Phosphate, Oligopeptide-20, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7, Tocopheryl Acetate, Panthenol, Allantoin, Magnesium Ascorbyl Phosphate, Tocopherol, Chlorella Vulgaris Extract, Caprylyl Glycol, Sodium Oleate, Glycine Soja (Soybean) Oil, Hydrogenated Phosphatidylcholine, Cellulose Gum, Sodium Lactate, Mica, Dimethiconol, Lecithin, Polymethyl Methacrylate, Microcrystalline Cellulose, Aminomethyl Propanol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Polysorbate 60, Parfum (Fragrance), Carbomer, Polysorbate 20, Sodium PCA, Phenoxyethanol, Citric Acid, Chlorphenesin, Disodium EDTA, Cyclohexasiloxane, Linalool, Citronellol, Limonene, Hexyl Cinnamal, CI 77891 (Titanium Dioxide).

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.
Purpose Sunscreen

Spl product data elements

Usually a list of ingredients in a drug product.
Intensite Creme Lustre Day SPF 30 US AVOBENZONE, OCTISALATE, OCTOCRYLENE WATER SUNFLOWER OIL CYCLOMETHICONE 5 UNDECYLCRYLENE DIMETHICONE (10000 MW) BUTYLOCTYL SALICYLATE BUTYLENE GLYCOL CETOSTEARYL ALCOHOL C13-15 ALKANE GLYCERIN SORBITAN MONOSTEARATE PPG-2 MYRISTYL ETHER PROPIONATE POTASSIUM CETYL PHOSPHATE PALMITOYL TRIPEPTIDE-1 PALMITOYL TETRAPEPTIDE-7 .ALPHA.-TOCOPHEROL ACETATE PANTHENOL ALLANTOIN MAGNESIUM ASCORBYL PHOSPHATE TOCOPHEROL CHLORELLA VULGARIS CAPRYLYL GLYCOL SODIUM OLEATE SOYBEAN OIL CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED SODIUM LACTATE MICA MICROCRYSTALLINE CELLULOSE AMINOMETHYLPROPANOL POLYSORBATE 60 CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE POLYSORBATE 20 SODIUM PYRROLIDONE CARBOXYLATE PHENOXYETHANOL CITRIC ACID MONOHYDRATE CHLORPHENESIN EDETATE DISODIUM ANHYDROUS CYCLOMETHICONE 6 LINALOOL, (+/-)- .BETA.-CITRONELLOL, (R)- LIMONENE, (+)- .ALPHA.-HEXYLCINNAMALDEHYDE TITANIUM DIOXIDE AVOBENZONE AVOBENZONE OCTISALATE OCTISALATE OCTOCRYLENE OCTOCRYLENE

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.
Package Labeling: Outer Package3 Inner Package3 Box2 Package Labeling: Sample2 Sample02

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 Other information Protect the product in this container from excessive heat and direct sun.

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 or comments? Call , M – F 8am – 5pm CST. 1-866-986-7083

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.

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