Hampton Sun SPF 50

AVOBENZONE 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 % TOPICAL HUMAN OTC DRUG

Hampton Sun SPF 50 is an FDA drug label for the active ingredient AVOBENZONE 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 % manufactured by S&C Hampton Sun LLC 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 20260518.

Generic name
AVOBENZONE 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 %
Manufacturer
S&C Hampton Sun LLC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87170-020
Application
M020
Label effective
20260518

About this product

Hampton Sun SPF 50 is an FDA-registered drug product whose active ingredient is AVOBENZONE 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 %. It is labelled by S&C Hampton Sun LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87170-020, application M020, label effective 20260518. It is one of 2 FDA drug label records sharing the active ingredient AVOBENZONE 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 %. 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 AVOBENZONE 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 % are most often described in connection with: helps prevent, sunburn higher, spf gives, sun protection. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredients Avobenzone 3.00 % Octisalate 5.00 % Homosalate 10.00 %

Indications & Usage

Uses: Helps prevent sunburn, higher SPF gives more sun protection

More products with the same ingredient

AVOBENZONE 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 %

Hampton Sun SPF 30

S&C Hampton Sun LLC View label

How products containing AVOBENZONE 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 % compare

FDA lists 2 drug label records with AVOBENZONE 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 % 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
— — S&C Hampton Sun LLC 2
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Frequently asked questions

What is Hampton Sun SPF 50 used for?
Uses: Helps prevent sunburn, higher SPF gives more sun protection

Who makes Hampton Sun SPF 50?
S&C Hampton Sun LLC is the labeler of record for Hampton Sun SPF 50. 2 FDA label records share the active ingredient AVOBENZONE 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 %, 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 Hampton Sun SPF 50 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 Hampton Sun SPF 50 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 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 %?
Yes. 2 FDA drug label records list AVOBENZONE 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 % 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 Hampton Sun SPF 50 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.