Jack Black Intense Lip Therapy SPF25, Natural Mint and Shea Butter
Jack Black Intense Lip Therapy SPF25, Natural Mint and Shea Butter is an FDA drug label for the active ingredient LIP BALM 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
- LIP BALM SUNSCREEN
- Manufacturer
- Jack Black, LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 66738-300
- Application
- M020
- Label effective
- 20260908
About this product
Jack Black Intense Lip Therapy SPF25, Natural Mint and Shea Butter is an FDA-registered drug product whose active ingredient is LIP BALM SUNSCREEN. It is labelled by Jack Black, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 66738-300, application M020, label effective 20260908. It is one of 5 FDA drug label records sharing the active ingredient LIP BALM 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 LIP BALM SUNSCREEN are most often described in connection with: helps prevent, chapped lips. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use Helps prevent sunburn and chapped lips.
Dosage & Administration
Directions Apply liberally 15 minutes before sun exposure and as needed. Children under 6 months: ask a doctor.
Warnings
Warnings Stop use if skin rash occurs.
More products with the same ingredient
LIP BALM SUNSCREENJack Black Intense Lip Therapy SPF25, Black Tea and Blackberry
View labelJack Black Intense Thearpy Lip Balm SPF25, Lemon and Shea Butter
View labelJack Black Intense Therapy Lip Balm SPF25, Grapefruit and Ginger
View labelJack Black Lavender Lip Balm 0.25oz
View labelHow products containing LIP BALM SUNSCREEN compare
FDA lists 5 drug label records with LIP BALM 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 |
|---|---|---|---|
| — | — | Jack Black, LLC | 4 |
| — | — | Jack Black, L.L.C. | 1 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is Jack Black Intense Lip Therapy SPF25, Natural Mint and Shea Butter used for?
Use Helps prevent sunburn and chapped lips.
Who makes Jack Black Intense Lip Therapy SPF25, Natural Mint and Shea Butter?
Jack Black, LLC is the labeler of record for Jack Black Intense Lip Therapy SPF25, Natural Mint and Shea Butter. 5 FDA label records share the active ingredient LIP BALM 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 Intense Lip Therapy SPF25, Natural Mint and Shea Butter 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 Intense Lip Therapy SPF25, Natural Mint and Shea Butter 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 LIP BALM SUNSCREEN?
Yes. 5 FDA drug label records list LIP BALM 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 Intense Lip Therapy SPF25, Natural Mint and Shea Butter 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.