Everyday Sheer Coverage Medium Tint SPF 20

ZINC OXIDE TOPICAL HUMAN OTC DRUG

Everyday Sheer Coverage Medium Tint SPF 20 is an FDA drug label for the active ingredient ZINC OXIDE manufactured by Allure Labs Inc 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 20171220.

Generic name
ZINC OXIDE
Manufacturer
Allure Labs Inc
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
62742-4160
Application
part352
Label effective
20171220

About this product

Everyday Sheer Coverage Medium Tint SPF 20 is an FDA-registered drug product whose active ingredient is ZINC OXIDE. It is labelled by Allure Labs Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 62742-4160, application part352, label effective 20171220. It is one of 404 FDA drug label records sharing the active ingredient 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.

What it is used for

Across FDA labelling, products containing ZINC OXIDE are most often described in connection with: sun protection, product reduces, risk cancer, early skin, helps prevent. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Non Nano Zinc Oxide - 17.7%

Indications & Usage

Uses: if used as directed with other sun protection measures, this product reduces the risk of cancer, early skin aging and helps prevent sunburn.

Dosage & Administration

Shake well and keep in a cool place. Apply liberally to face, neck and chest before sun exposure. Reapply as needed, and after swimming, perspirin or towel drying. For children under 6 months, consult physicain.

Warnings

for external use only. if irritation developes, discontinue use and consult physician.

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How products containing ZINC OXIDE compare

FDA lists 404 drug label records with 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.

Dosage formProductsManufacturerProducts
— — Ilia, Inc. 30
— — COSMAX USA, CORP 24
— — Colorescience 16
— — Allure Labs Inc 9
— — Raw Elements LLC 9

Frequently asked questions

What is Everyday Sheer Coverage Medium Tint SPF 20 used for?
Uses: if used as directed with other sun protection measures, this product reduces the risk of cancer, early skin aging and helps prevent sunburn.

Who makes Everyday Sheer Coverage Medium Tint SPF 20?
Allure Labs Inc is the labeler of record for Everyday Sheer Coverage Medium Tint SPF 20. 404 FDA label records share the active ingredient 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 Everyday Sheer Coverage Medium Tint SPF 20 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 Everyday Sheer Coverage Medium Tint SPF 20 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 ZINC OXIDE?
Yes. 404 FDA drug label records list 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 Everyday Sheer Coverage Medium Tint SPF 20 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.