Neutrogena Clear Face Sunscreen Acne Prone Skin Broad Spectrum SPF 60

AVOBENZONE, BEMOTRIZINOL, HOMOSALATE, OCTISALATE TOPICAL HUMAN OTC DRUG

Neutrogena Clear Face Sunscreen Acne Prone Skin Broad Spectrum SPF 60 is an FDA drug label for the active ingredient AVOBENZONE, BEMOTRIZINOL, HOMOSALATE, OCTISALATE 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 20260812.

Generic name
AVOBENZONE, BEMOTRIZINOL, HOMOSALATE, OCTISALATE
Manufacturer
Kenvue Brands LLC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
69968-1015
Application
M020
Label effective
20260812

About this product

Neutrogena Clear Face Sunscreen Acne Prone Skin Broad Spectrum SPF 60 is an FDA-registered drug product whose active ingredient is AVOBENZONE, BEMOTRIZINOL, HOMOSALATE, OCTISALATE. It is labelled by Kenvue Brands LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 69968-1015, application M020, label effective 20260812. It is one of 2 FDA drug label records sharing the active ingredient AVOBENZONE, BEMOTRIZINOL, HOMOSALATE, OCTISALATE. 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, BEMOTRIZINOL, HOMOSALATE, OCTISALATE 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 Avobenzone (3%), Bemotrizinol (6%), Homosalate (15%), Octisalate (5%)

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 For sunscreen use: ● apply generously and evenly 15 minutes before sun exposure ● reapply 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 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.

More products with the same ingredient

AVOBENZONE, BEMOTRIZINOL, HOMOSALATE, OCTISALATE

Neutrogena Ultra Sheer Daily Face Sunscreen Broad Spectrum SPF 70

Kenvue Brands LLC View label

How products containing AVOBENZONE, BEMOTRIZINOL, HOMOSALATE, OCTISALATE compare

FDA lists 2 drug label records with AVOBENZONE, BEMOTRIZINOL, HOMOSALATE, OCTISALATE 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
— — Kenvue Brands LLC 2
— — — —
— — — —
— — — —
— — — —

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 Clear Face Sunscreen Acne Prone Skin Broad Spectrum SPF 60 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 Clear Face Sunscreen Acne Prone Skin Broad Spectrum SPF 60?
Kenvue Brands LLC is the labeler of record for Neutrogena Clear Face Sunscreen Acne Prone Skin Broad Spectrum SPF 60. 2 FDA label records share the active ingredient AVOBENZONE, BEMOTRIZINOL, HOMOSALATE, OCTISALATE, 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 Clear Face Sunscreen Acne Prone Skin Broad Spectrum SPF 60 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 Clear Face Sunscreen Acne Prone Skin Broad Spectrum SPF 60 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, BEMOTRIZINOL, HOMOSALATE, OCTISALATE?
Yes. 2 FDA drug label records list AVOBENZONE, BEMOTRIZINOL, HOMOSALATE, OCTISALATE 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 Clear Face Sunscreen Acne Prone Skin Broad Spectrum SPF 60 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.