Standard Procedure SPF 50 Sunscreen Face and Body

Standard Procedure SPF 50 Sunscreen Face and Body is an FDA-registered drug product whose active ingredient is AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE. It is labelled by Baxter Laboratories taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 70157-027, application M020, label effective 20260513. It is one of 105 FDA drug label records sharing the active ingredient AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE. 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 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE are most often described in connection with: ask doctor, rash occurs. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Stop use and ask a doctor if rash occurs

Directions Apply generously and evenly Reapply after 80 minutes of swimming Immediately after towel drying at least every 2 hours use a water resistant sunscreen if swimming or sweating Sun Protection Measures . Spending time in the sun increases your risk of skin cancer and early skin aging.To decrease this risk, regularly use a sunscreen with broad spectrum SPF 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m. to 2 p.m. wear long-sleeve shirts, pants, hats, and sunglasses Children under 6 months: ask a doctor

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.

FDA lists 105 drug label records with AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE 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 Standard Procedure SPF 50 Sunscreen Face and Body used for?
Stop use and ask a doctor if rash occurs

Who makes Standard Procedure SPF 50 Sunscreen Face and Body?
Baxter Laboratories is the labeler of record for Standard Procedure SPF 50 Sunscreen Face and Body. 105 FDA label records share the active ingredient AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 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 Standard Procedure SPF 50 Sunscreen Face and Body 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 Standard Procedure SPF 50 Sunscreen Face and Body 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 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE?
Yes. 105 FDA drug label records list AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE 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 Standard Procedure SPF 50 Sunscreen Face and Body 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.