Neutrogena Collagen Bank SPF Moisturizer Sunscreen Broad Spectrum SPF 30
Neutrogena Collagen Bank SPF Moisturizer Sunscreen Broad Spectrum SPF 30 is an FDA drug label for the active ingredient AVOBENZONE, HOMOSALATE, OCTISALATE, 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 20260624.
- Generic name
- AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
- Manufacturer
- Kenvue Brands LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 69968-0931
- Application
- M020
- Label effective
- 20260624
About this product
Neutrogena Collagen Bank SPF Moisturizer Sunscreen Broad Spectrum SPF 30 is an FDA-registered drug product whose active ingredient is AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE. It is labelled by Kenvue Brands LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 69968-0931, application M020, label effective 20260624. 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.
What it is used for
Across FDA labelling, products containing AVOBENZONE, HOMOSALATE, OCTISALATE, 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
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
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AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEAVON ANEW SOLAIRE EVERYDAY FACE PROTECTION BROAD SPECTRUM SPF 50 SUNSCREEN
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View labelAveeno Daily Moisturizing Face Sunscreen Broad Spectrum SPF30
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View labelHow products containing AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE compare
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.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Sun Life Brands, LLC | 9 |
| — | — | TARGET CORPORATION | 9 |
| — | — | Meijer Distribution, Inc. | 4 |
| — | — | COOLA LLC | 3 |
| — | — | Derma Care Research Labs, LLC | 3 |
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.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| 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 Collagen Bank SPF Moisturizer 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 Collagen Bank SPF Moisturizer Sunscreen Broad Spectrum SPF 30?
Kenvue Brands LLC is the labeler of record for Neutrogena Collagen Bank SPF Moisturizer Sunscreen Broad Spectrum SPF 30. 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 Neutrogena Collagen Bank SPF Moisturizer 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 Collagen Bank SPF Moisturizer 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, 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 Neutrogena Collagen Bank SPF Moisturizer 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.