WILMA SCHUMANN Moisture Protektiv Day Cream SPF-20

OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE TOPICAL HUMAN OTC DRUG

WILMA SCHUMANN Moisture Protektiv Day Cream SPF-20 is an FDA drug label for the active ingredient OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE manufactured by SKINMETICS 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 20231111.

Generic name
OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE
Manufacturer
SKINMETICS INC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
82329-247
Application
M020
Label effective
20231111

About this product

WILMA SCHUMANN Moisture Protektiv Day Cream SPF-20 is an FDA-registered drug product whose active ingredient is OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE. It is labelled by SKINMETICS INC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 82329-247, application M020, label effective 20231111. 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 OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE are most often described in connection with: helps prevent, sun protection, measures see, risk skin, aging caused. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredients Octinoxate 6% Oxybenzone 3% Titanium Dioxide 3% Purpose Sunscreen

Indications & Usage

Uses helps prevent sunburn if used as directed with other sun protection measures (see ), decreases the risk of skin cancer and early skin aging caused by the sun. Directions

Dosage & Administration

Directions: apply liberally 15 minutes before sun exposure use a water resistant sunscreen if swimming or sweating. immediately after swimming or sweating immediately after towel drying at least every 2 hours 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 of 15 or higher and other sun protection measures including: Sun Protection Measures. limit time in the sun, especially from 10 a.m. 0 2 p.m. wear long-sleeve shirts, pants, hats, and sunglasses children under 6 months: Ask a doctor reapply:

Warnings

Warnings For external use only Do not ues on damaged or broken skin When using this product keep out of the 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.

Frequently asked questions

What is WILMA SCHUMANN Moisture Protektiv Day Cream SPF-20 used for?
Uses helps prevent sunburn if used as directed with other sun protection measures (see ), decreases the risk of skin cancer and early skin aging caused by the sun. Directions

Who makes WILMA SCHUMANN Moisture Protektiv Day Cream SPF-20?
SKINMETICS INC is the labeler of record for WILMA SCHUMANN Moisture Protektiv Day Cream SPF-20.

What form does WILMA SCHUMANN Moisture Protektiv Day Cream 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 WILMA SCHUMANN Moisture Protektiv Day Cream 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.

Has WILMA SCHUMANN Moisture Protektiv Day Cream 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.