Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUS

Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUS is an FDA-registered drug product whose active ingredient is HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE. It is labelled by ATOMY CO., LTD. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 52257-1420, application M020, label effective 20260602. It is one of 2 FDA drug label records sharing the active ingredient HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE are most often described in connection with: helps prevent, sun protection, measures see, directions decreases, risk skin, aging caused, information protect, excessive heat. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

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 Other Information: Protect this product from excessive heat and direct sun

Directions: • Apply liberally 15 minutes before sun exposure • Reapply at least every 2 hours • Use a water-resistant sunscreen if swimming or sweating • 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-sleeved shirts, pants, hats, and sunglasses

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.

FDA lists 2 drug label records with HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUS used for?
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 Other Information: Protect this product from excessive heat and direct sun

Who makes Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUS?
ATOMY CO., LTD. is the labeler of record for Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUS. 2 FDA label records share the active ingredient HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUS come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUS prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE?
Yes. 2 FDA drug label records list HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUS been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.