EELHOE Sunscreen

TITANIUM DIOXIDE TOPICAL HUMAN OTC DRUG

EELHOE Sunscreen is an FDA drug label for the active ingredient TITANIUM DIOXIDE manufactured by Shantou Eelhoe Daily Chemical Technology Co., Ltd. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260511.

Generic name
TITANIUM DIOXIDE
Manufacturer
Shantou Eelhoe Daily Chemical Technology Co., Ltd.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
85064-028
Application
M020
Label effective
20260511

About this product

EELHOE Sunscreen is an FDA-registered drug product whose active ingredient is TITANIUM DIOXIDE. It is labelled by Shantou Eelhoe Daily Chemical Technology Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85064-028, application M020, label effective 20260511. It is one of 71 FDA drug label records sharing the active ingredient TITANIUM DIOXIDE. 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.

What it is used for

Across FDA labelling, products containing TITANIUM DIOXIDE are most often described in connection with: take appropriate, amount sunscreen, skin care, routine apply, evenly areas, susceptible radiation. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ETHYLHEXYL METHOXYCINNAMATE、OCTOCRYLENE、TITANIUM DIOXIDE

Indications & Usage

1. Take an appropriate amount of sunscreen at the end of your skin care routine. 2. Apply evenly to areas susceptible to UV radiation. 3. Wipe evenly.

Dosage & Administration

1. Take an appropriate amount of sunscreen at the end of your skin care routine. 2. Apply evenly to areas susceptible to UV radiation. 3. Wipe evenly.

Warnings

Please keep out of reach of children. Do not swallow. Please clean your hands before use to ensure the best results from the product. Discontinue use if signs of irritation or rash occur. Store in a cool and dry place.

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TITANIUM DIOXIDE

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How products containing TITANIUM DIOXIDE compare

FDA lists 71 drug label records with TITANIUM DIOXIDE 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.

Dosage formProductsManufacturerProducts
— — Amway Corp 16
— — Farmasi US LLC 12
— — Orveon Global US LLC 7
— — TAN ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI 4
— — 3LAB, Inc 3

Frequently asked questions

What is EELHOE Sunscreen used for?
1. Take an appropriate amount of sunscreen at the end of your skin care routine. 2. Apply evenly to areas susceptible to UV radiation. 3. Wipe evenly.

Who makes EELHOE Sunscreen?
Shantou Eelhoe Daily Chemical Technology Co., Ltd. is the labeler of record for EELHOE Sunscreen. 71 FDA label records share the active ingredient TITANIUM DIOXIDE, 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 EELHOE 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 EELHOE 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 TITANIUM DIOXIDE?
Yes. 71 FDA drug label records list TITANIUM DIOXIDE 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 EELHOE 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.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.