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Your name cosmetics brightening cc cream broad spectrum spf 20 - Medication Information

Product NDC Code 59735-160
Drug Name

Your name cosmetics brightening cc cream broad spectrum spf 20

Type Generic
Active Ingredients
Octinoxate 7.5 g/100g
Titanium dioxide 5 g/100g
Zinc oxide .99 g/100g
Route TOPICAL
Dosage Form LOTION
Application Number part352
Labeler Name Mana Products
Packages
Package NDC Code Description
59735-160-01 1 tube in 1 carton (59735-160-01) / 33 g in 1 tube
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Octinoxate 7.5% Titanium Dioxide 5.00% Zinc Oxide 0.99%

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 at least every 2 hours Use water resistant sunscreen if swimming or sweathing Sun Protection Measures: Spending time in the sun decreases risk of skin cancer and early again. To decrease this risk, regulaory 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 10:00 am - 2:00 pm. Wear long sleeved shirts, pants, hats and sunglasses. Children under 6 months: ask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Aqua/Water/Eau, Dimethicone, Glycerin, PEG/PPG-18/18 Dimethicone, Butylene Glycol, Trimethylsiloxysilicate , Saccharide Isomerate, Tocopherol, Ascorbyl Palmitate, Rose Extract, Caprylic/Capric Triglyceride, Octyldodecyl Neopentanoate , Ethylhexyl Palmitate, Nylon-12, Boron Nitride, Dextrin Palmitate, Sodium Chloride, Aluminum Hydroxide, Polymethylsilsesquioxane, Glyceryl Polyacrylate, HDI/Trimethylol Hexyllactone Crosspolymer, Dimethylmethoxy Chromanyl Palmitate, Phytosteryl/Isostearyl/Cetyl/Stearyl/Behenyl Dimer Dilinoleate, Benzimidazole Diamond Amidoethyl Urea Carbamoyl Propyl Polymethylsilsesquioxane, Calcium Silicate, Palmitic Acid, Stearic Acid, Citric Acid , Lecithin, Acrylates/Ammonium Methacrylate Copolymer, Sodium Citrate, Triethyl Citrate , Acrylates Crosspolymer, Disteardimonium Hectorite, Xanthan Gum, Alcohol, Alcohol Denat., Methicone, Triethoxycaprylylsilane, Lysine, Potassium Chloride, Magnesium Chloride, Zinc Chloride, Sodium Hyaluronate, Sodium Dehydroacetate, Magnesium Ascorbyl Phosphate, Octyldodecanol, Potassium Sorbate, Disodium EDTA, Caprylyl Glycol, Hexylene Glycol, Phenoxyethanol May Contain (+/-): Mica, Titanium Dioxide (CI 77891), 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.
Use 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.
Your Name Cosmetics Brightening CC Cream Broad Spectrum SPF 20 Your Name Cosmetics Brightening CC Cream Broad Spectrum SPF 20 WATER DIMETHICONE GLYCERIN PEG/PPG-18/18 DIMETHICONE BUTYLENE GLYCOL TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) SACCHARIDE ISOMERATE TOCOPHEROL ASCORBYL PALMITATE CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE OCTYLDODECYL NEOPENTANOATE ETHYLHEXYL PALMITATE NYLON-12 BORON NITRIDE DEXTRIN PALMITATE (CORN; 20000 MW) SODIUM CHLORIDE ALUMINUM HYDRIDE POLYMETHYLSILSESQUIOXANE (11 MICRONS) DIMETHYLMETHOXY CHROMANYL PALMITATE PHYTOSTERYL/ISOSTEARYL/CETYL/STEARYL/BEHENYL DIMER DILINOLEATE CALCIUM SILICATE PALMITIC ACID STEARIC ACID CITRIC ACID MONOHYDRATE LECITHIN, SOYBEAN SODIUM CITRATE TRIETHYL CITRATE DISTEARDIMONIUM HECTORITE XANTHAN GUM ALCOHOL METHICONE (20 CST) TRIETHOXYCAPRYLYLSILANE LYSINE POTASSIUM CHLORIDE MAGNESIUM CHLORIDE ZINC CHLORIDE SODIUM DEHYDROACETATE MAGNESIUM ASCORBYL PHOSPHATE OCTYLDODECANOL POTASSIUM SORBATE DISODIUM EDTA-COPPER CAPRYLYL GLYCOL HEXYLENE GLYCOL PHENOXYETHANOL OCTINOXATE OCTINOXATE TITANIUM DIOXIDE TITANIUM DIOXIDE 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.
Principal Display Panel 59735-160-01

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 form excessive heat and direct sun

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