Jack Black Sun Guard Sunscreen SPF45
Jack Black Sun Guard Sunscreen SPF45 is an FDA drug label for the active ingredient SUNSCREEN manufactured by Jack Black, 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 20260908.
- Generic name
- SUNSCREEN
- Manufacturer
- Jack Black, LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 66738-304
- Application
- M020
- Label effective
- 20260908
About this product
Jack Black Sun Guard Sunscreen SPF45 is an FDA-registered drug product whose active ingredient is SUNSCREEN. It is labelled by Jack Black, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 66738-304, application M020, label effective 20260908. It is one of 10 FDA drug label records sharing the active ingredient SUNSCREEN. 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 SUNSCREEN are most often described in connection with: helps prevent. 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
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 two hours Children under 6 months: ask a doctor Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with a broad spectrum SFP value of 15 or higher Limit time in the sun, eespecially from 10 a.m. - 2 p.m.
Warnings
Warnings For external use only Do not use on damaged or broken skin Stop use and ask doctor if rash occurs When using this product keep out of eyes Rinse with water to remove Keep out of reach of children If swallowed, get medical help or contact Poison Control Cneter right away
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View labelQ Skin Science
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View labelHow products containing SUNSCREEN compare
FDA lists 10 drug label records with SUNSCREEN 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 |
|---|---|---|---|
| — | — | Swiss-American CDMO, LLC | 2 |
| — | — | Dr. Natural LLC | 1 |
| — | — | Earth Baby, Inc. | 1 |
| — | — | Guangzhou Oupeng Cosmetics Co., Ltd. | 1 |
| — | — | International Cosmeceuticals, Inc | 1 |
Frequently asked questions
What is Jack Black Sun Guard Sunscreen SPF45 used for?
Uses Helps prevent sunburn
Who makes Jack Black Sun Guard Sunscreen SPF45?
Jack Black, LLC is the labeler of record for Jack Black Sun Guard Sunscreen SPF45. 10 FDA label records share the active ingredient SUNSCREEN, 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 Jack Black Sun Guard Sunscreen SPF45 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 Jack Black Sun Guard Sunscreen SPF45 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 SUNSCREEN?
Yes. 10 FDA drug label records list SUNSCREEN 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 Jack Black Sun Guard Sunscreen SPF45 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.