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Radiance foundation broad spectrum spf 20 - honey - Medication Information

Product NDC Code 68828-730
Drug Name

Radiance foundation broad spectrum spf 20 - honey

Type Brand
Active Ingredients
Octinoxate 3 g/100ml
Zinc oxide 6.8 g/100ml
Route TOPICAL
Dosage Form LIQUID
Application Number part352
Labeler Name JAFRA COSMETICS INTERNATIONAL
Packages
Package NDC Code Description
68828-730-01 1 bottle in 1 carton (68828-730-01) / 30 ml in 1 bottle
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredients Purpose Octinoxate 3% .................. Sunscreen Zinc Oxide 6.8% ................ 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 use a water resistant sunscreen if swimming or sweating reapply at least every 2 hours children under 6 months: Ask a doctor 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-sleeve shirts, pants, hats, and sunglasses

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Water/Aqua, Titanium Dioxide, Triethoxycaprylylsilane, Caprylic Capric Triglyceride, Polyhydroxystearic Acid, Cyclomethicone, Hydroxypropylcocoate PEG-8 Dimethicone, C12-15 Alkyl Benzoate, Phenyl Dimethicone, Phenyl Trimethicone, Cyclopentasiloxane, Dimethicone/Vinyl Dimethicone Crosspolymer, Squalane, Di-PPG-3 Myristyl Ether Adipate, Caprylyl Methicone, Dimethicone, PEG-10 Dimethicone, Disteardimonium Hectorite, Boron Nitride, Royal Jelly, Propanediol, Sodium Chloride, DMDM Hydantoin, Dextrin Palmitate, Oryza Sativa (Rice) Bran Extract, Rosamarinus Officinalis (Rosemary) Leaf Extract, Helianthus Annuus (Sunflower) Extract, Tocopherol, Panthenol, Tocopheryl Acetate, PEG-4 Laurate, Iodopropynyl Butylcarbamate, Withania Somniferia (Winter Cherry) Extract, Nelumbo Nucifera (Lotus) Extract, Biosaccharide Gum-4, Chondrus Crispus (Carrageenan) Extract, Smithsonite Extract, Iron Oxides/CI 77491/CI 77492/CI 77499

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

Spl product data elements

Usually a list of ingredients in a drug product.
Radiance Foundation Broad Spectrum SPF 20 - Honey Octinoxate, Zinc Oxide WATER TITANIUM DIOXIDE TRIETHOXYCAPRYLYLSILANE POLYHYDROXYSTEARIC ACID (2300 MW) CYCLOMETHICONE HYDROXYPROPYLCOCOATE PEG-8 DIMETHICONE ALKYL (C12-15) BENZOATE PHENYL TRIMETHICONE CYCLOMETHICONE 5 DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) SQUALANE DI-PPG-3 MYRISTYL ETHER ADIPATE CAPRYLYL TRISILOXANE DIMETHICONE PEG-10 DIMETHICONE (600 CST) DISTEARDIMONIUM HECTORITE BORON NITRIDE ROYAL JELLY PROPANEDIOL SODIUM CHLORIDE DMDM HYDANTOIN RICE BRAN ROSEMARY HELIANTHUS ANNUUS FLOWERING TOP TOCOPHEROL PANTHENOL .ALPHA.-TOCOPHEROL ACETATE PEG-4 LAURATE IODOPROPYNYL BUTYLCARBAMATE BIOSACCHARIDE GUM-4 CHONDRUS CRISPUS CARRAGEENAN FERRIC OXIDE RED FERRIC OXIDE YELLOW FERROSOFERRIC OXIDE MEDIUM-CHAIN TRIGLYCERIDES DEXTRIN PALMITATE (CORN; 20000 MW) WITHANIA SOMNIFERA ROOT OCTINOXATE OCTINOXATE ZINC OXIDE ZINC OXIDE

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.
Product label image description

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

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 o n damaged or broken skin Stop use and ask a doctor if rash occurs When using this product keep out of eyes. Rinse with water to remove. Keep out of reach of children. If product is 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