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Sun bum spf 15 premium moisturizing sunscreen - Medication Information

Product NDC Code 69039-212
Drug Name

Sun bum spf 15 premium moisturizing sunscreen

Type Brand
Active Ingredients
Avobenzone 20 mg/ml
Homosalate 50 mg/ml
Octisalate 20 mg/ml
Octocrylene 100 mg/ml
Route TOPICAL
Dosage Form LOTION
Application Number part352
Labeler Name Sun Bum, LLC.
Packages
Package NDC Code Description
69039-212-03 3780 ml in 1 bottle (69039-212-03)
69039-212-01 1 bottle in 1 box (69039-212-01) / 237 ml in 1 bottle
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredients Avobenzone 2%, Homosalate 5%, Octisalate 2%, Octocrylene 10% 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 • 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 Broad Spectrum SPF of 15 or higher and other sun protection measures, including: • Limit time in the sun, especially from 10 am - 2 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 water, butyloctylsalicylate, hydratedsilica, styrene/acrylatescopolymer, dimethicone, VP/hexadecene copolymer, polyester-8, caprylyl methicone, ethylhexyl stearate, trideceth-6, glyceryl stearate, PEG-100 stearate, fragrance, sodium polyacrylate, behenyl alcohol, dimethyl capramide, ethylhexylglycerin, trimethylsiloxysilicate, xanthan gum, polyaminopropyl biguanide, tocopheryl acetate, BHT, disodium EDTA, methylisothiazolinone

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 • higher SPF gives more sunburn protection • Ifusedasdirectedwithothersunprotectionmeasures(seeDirections), decreasestheriskofskincancerandearlyskinagingcausedbythesun

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.
SUN BUM SPF 15 PREMIUM MOISTURIZING SUNSCREEN AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE WATER BUTYLOCTYL SALICYLATE HYDRATED SILICA STYRENE DIMETHICONE VINYLPYRROLIDONE/HEXADECENE COPOLYMER CAPRYLYL TRISILOXANE ETHYLHEXYL STEARATE TRIDECETH-6 GLYCERYL MONOSTEARATE POLYETHYLENE GLYCOL 4500 DOCOSANOL DIMETHYL CAPRAMIDE ETHYLHEXYLGLYCERIN XANTHAN GUM POLYAMINOPROPYL BIGUANIDE .ALPHA.-TOCOPHEROL ACETATE BUTYLATED HYDROXYTOLUENE EDETATE DISODIUM ANHYDROUS METHYLISOTHIAZOLINONE AVOBENZONE AVOBENZONE HOMOSALATE HOMOSALATE 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: Label

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 Otherinformation protectthis product 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 product is 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? 1-877-978-6286

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 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