MENS SPF50 ALL IN ONE SUNSCREEN

MENS SPF50 ALL IN ONE SUNSCREEN CUTANEOUS HUMAN OTC DRUG

MENS SPF50 ALL IN ONE SUNSCREEN is an FDA drug label for the active ingredient MENS SPF50 ALL IN ONE SUNSCREEN manufactured by Lance (Guangzhou) Biological Technology Co., Ltd. administered by CUTANEOUS. 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 20260720.

Generic name
MENS SPF50 ALL IN ONE SUNSCREEN
Manufacturer
Lance (Guangzhou) Biological Technology Co., Ltd.
Product type
HUMAN OTC DRUG
Route
CUTANEOUS
Dosage form
N/A
NDC
87593-101
Application
M020
Label effective
20260720

About this product

MENS SPF50 ALL IN ONE SUNSCREEN is an FDA-registered drug product whose active ingredient is MENS SPF50 ALL IN ONE SUNSCREEN. It is labelled by Lance (Guangzhou) Biological Technology Co., Ltd. taken by cutaneous and marketed as a human otc drug product. Identifiers on file: NDC 87593-101, application M020, label effective 20260720. 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 MENS SPF50 ALL IN ONE SUNSCREEN are most often described in connection with: indications usage. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Indications & Usage

INDICATIONS USAGE SECTION INDICATIONS USAGE SECTION INDICATIONS USAGE SECTION

Dosage & Administration

DOSAGE ADMINISTRATION SECTION DOSAGE ADMINISTRATION SECTION DOSAGE ADMINISTRATION SECTION

Warnings

WARNINGS SECTION WARNINGS SECTION WARNINGS SECTION

Frequently asked questions

What is MENS SPF50 ALL IN ONE SUNSCREEN used for?
INDICATIONS USAGE SECTION INDICATIONS USAGE SECTION INDICATIONS USAGE SECTION

Who makes MENS SPF50 ALL IN ONE SUNSCREEN?
Lance (Guangzhou) Biological Technology Co., Ltd. is the labeler of record for MENS SPF50 ALL IN ONE SUNSCREEN.

What form does MENS SPF50 ALL IN ONE SUNSCREEN come in?
administered by cutaneous. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is MENS SPF50 ALL IN ONE 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.

Has MENS SPF50 ALL IN ONE 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.