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Product NDC Code | 30142-241 | ||||||
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Drug Name | Kroger shimmer sunscreen hydrating spf 40 |
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Type | Brand | ||||||
Active Ingredients |
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Route | TOPICAL | ||||||
Dosage Form | CREAM | ||||||
Application Number | M020 | ||||||
Labeler Name | THE KROGER COMPANY | ||||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredients Acobenzone 3.0%, Octisalate 5.0%, Octocrylene 10.0%
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 children under 6 months of age: Ask a doctor Sun Protection Measures . Spending time in the sun increases your risk of skin cancer and early aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum value of 15 or higher and other sun protection measures including: • limit time in the sun, especially from 10am-2pm • wear long-sleeved shirts, pants, hats, and sunglasses.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredient(s) acrylates/C10-30 alkyl acrylate crosspolymer, L-arginine, bismuth oxychloride, butyloctyl salicylate, C12-15 alkyl benzoate, calcium pantothenate, caprylic/capric triglyceride, caprylyl glycol, cetyl phosphate, chlorphenesin, coco-caprylate/caprate, diisopropyl sebacate, ethylhexyl hydroxystearate, ferulic acid, glycerin, glyceryl stearate, helianthus annuus (sunflower) flower extract, 1,2-hexanediol, hydroxyacetophenone, iron oxides, isodecyl neopentanoate, isododecane, lauryl lactate, limonium gerberi extract, mica, niacinamide, phospholipids, polymethylsilsesquioxane, propanediol, sodium hyaluronate, theobroma cacao (cocoa) seed extract, titanium dioxide, tocopherol, triethoxycaprylylsilane, trisodium ethylenediamine disuccinate, water
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.Kroger Shimmer Sunscreen Hydrating SPF 40 AVOBENZONE, OCTISALATE, OCTOCRYLENE COCO-CAPRYLATE/CAPRATE ETHYLHEXYL HYDROXYSTEARATE WATER .ALPHA.-TOCOPHEROL, DL- AVOBENZONE AVOBENZONE OCTISALATE OCTISALATE OCTOCRYLENE OCTOCRYLENE MICA CAPRYLYL GLYCOL TITANIUM DIOXIDE FERRIC OXIDE YELLOW COCOA CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) FERULIC ACID LIMONIUM GERBERI FLOWERING TOP OMEGA-3 FATTY ACIDS TRISODIUM ETHYLENEDIAMINE DISUCCINATE BISMUTH OXYCHLORIDE STANNIC OXIDE BUTYLOCTYL SALICYLATE ALKYL (C12-15) BENZOATE CETYL PHOSPHATE CHLORPHENESIN DIISOPROPYL SEBACATE ISODODECANE ARGININE NIACINAMIDE PROPANEDIOL ISODECYL NEOPENTANOATE LAURYL LACTATE GLYCERIN GLYCERYL 1-STEARATE HELIANTHUS ANNUUS FLOWERING TOP HYDROXYACETOPHENONE PANTOTHENIC ACID POLYMETHYLSILSESQUIOXANE (11 MICRONS) HYALURONATE SODIUM TRIETHOXYCAPRYLYLSILANE 1,2-HEXANEDIOL
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.Label 01679K 01679A
Ask doctor
Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.Stop use and ask doctor if • rash occurs
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.
Other safety information
Information about safe use and handling of the product that may not have been specified in another field.Other Information protect the product in this container from excessive heat and direct sun may stain or damage some fabrics, materials or surfaces
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
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