MORANDIPARK PANTHENOL ULTRA LIGHT SUNSCREEN

MORANDIPARK PANTHENOL ULTRA LIGHT SUNSCREEN is an FDA-registered drug product whose active ingredient is HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE. It is labelled by BRAND GENOME CO., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87767-001, application M020, label effective 20260624. It is one of 12 FDA drug label records sharing the active ingredient HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE. 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, OCTOCRYLENE, OCTISALATE, AVOBENZONE are most often described in connection with: helps prevent, sun protection, measures see, directions decreases, risk skin, aging caused. 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.

Directions For sunscreen use ■ Apply liberally and evenly 15 minutes before sun exposure. ■ Reapply 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, regularty 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. ■ Children under 6 months of age: Ask a doctor ■ Use a water resistant sunscreen if swimming or sweating.

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 swallowed, get medical help or contact a Poison Control Center right away.

FDA lists 12 drug label records with HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE 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 MORANDIPARK PANTHENOL ULTRA LIGHT SUNSCREEN 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.

Who makes MORANDIPARK PANTHENOL ULTRA LIGHT SUNSCREEN?
BRAND GENOME CO., Ltd. is the labeler of record for MORANDIPARK PANTHENOL ULTRA LIGHT SUNSCREEN. 12 FDA label records share the active ingredient HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, 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 MORANDIPARK PANTHENOL ULTRA LIGHT SUNSCREEN 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 MORANDIPARK PANTHENOL ULTRA LIGHT SUNSCREEN 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, OCTOCRYLENE, OCTISALATE, AVOBENZONE?
Yes. 12 FDA drug label records list HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE 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 MORANDIPARK PANTHENOL ULTRA LIGHT SUNSCREEN 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.