Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 30

AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE TOPICAL HUMAN OTC DRUG

Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 30 is an FDA drug label for the active ingredient AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE manufactured by Kenvue Brands 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 20260910.

Generic name
AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE
Manufacturer
Kenvue Brands LLC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
69968-0552
Application
M020
Label effective
20260910

About this product

Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 30 is an FDA-registered drug product whose active ingredient is AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE. It is labelled by Kenvue Brands LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 69968-0552, application M020, label effective 20260910. It is one of 17 FDA drug label records sharing the active ingredient AVOBENZONE, HOMOSALATE, OCTISALATE, AND 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.

What it is used for

Across FDA labelling, products containing AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE are most often described in connection with: helps prevent, sun protection, measures see, directions decreases, 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 Purpose Avobenzone 2.5% Sunscreen Homosalate 6% Sunscreen Octisalate 4.5% Sunscreen Octocrylene 8% Sunscreen

Indications & Usage

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

Dosage & Administration

Directions apply liberally 15 minutes before sun exposure reapply: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours 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 a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m. – 2 p.m. wear long-sleeved shirts, pants, hats, and sunglasses children under 6 months of age: Ask a doctor

Warnings

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. Stop use and ask a doctor if rash occurs Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

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How products containing AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE compare

FDA lists 17 drug label records with AVOBENZONE, HOMOSALATE, OCTISALATE, AND 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.

Dosage formProductsManufacturerProducts
— — L'Oreal USA Products Inc 4
— — Kenvue Brands LLC 3
— — AHAVA Dead Sea Laboratories Ltd 1
— — CHANEL PARFUMS BEAUTE 1
— — ESTEE LAUDER INC 1

Recall and safety notices

1 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

RecallProductFirmClassStatusReported
D-0121-2026 TYLENOL, Acetaminophen, Extra Strength, 24 Caplets, 500mg each, distributed by: Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division, Fort Washington, PA 19034, NDC: 50580-378-04. Kenvue Brands LLC Class II Ongoing 20251105

Frequently asked questions

What is Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 30 used for?
Uses helps prevent sunburn if used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun

Who makes Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 30?
Kenvue Brands LLC is the labeler of record for Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 30. 17 FDA label records share the active ingredient AVOBENZONE, HOMOSALATE, OCTISALATE, AND 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 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 30 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 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 30 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, AND OCTOCRYLENE?
Yes. 17 FDA drug label records list AVOBENZONE, HOMOSALATE, OCTISALATE, AND 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 Neutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 30 been recalled?
1 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

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.