MEDULTIMA ADVENTURE SUNSCREEN
MEDULTIMA ADVENTURE SUNSCREEN is an FDA drug label for the active ingredient HOMOSALATE,OCTOCRYLENE, PHENYLBENZIMIDAZOLE SULFONIC ACID, ETHYLHEXYL SALICYLATE, BUTYL METHOXYDIBENZOYLMETHANE manufactured by Guangzhou Tata Biotechnology Co., Ltd. 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 20260604.
- Generic name
- HOMOSALATE,OCTOCRYLENE, PHENYLBENZIMIDAZOLE SULFONIC ACID, ETHYLHEXYL SALICYLATE, BUTYL METHOXYDIBENZOYLMETHANE
- Manufacturer
- Guangzhou Tata Biotechnology Co., Ltd.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 84066-109
- Application
- M020
- Label effective
- 20260604
About this product
MEDULTIMA ADVENTURE SUNSCREEN is an FDA-registered drug product whose active ingredient is HOMOSALATE,OCTOCRYLENE, PHENYLBENZIMIDAZOLE SULFONIC ACID, ETHYLHEXYL SALICYLATE, BUTYL METHOXYDIBENZOYLMETHANE. It is labelled by Guangzhou Tata Biotechnology Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 84066-109, application M020, label effective 20260604. 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 HOMOSALATE,OCTOCRYLENE, PHENYLBENZIMIDAZOLE SULFONIC ACID, ETHYLHEXYL SALICYLATE, BUTYL METHOXYDIBENZOYLMETHANE 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
helps prevent sunburn
Dosage & Administration
Directions • Apply liberally to face and neck 15 minutes before sun exposure • Use a water-resistant sunscreen if swimming or sweating • Reapply 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 of 15 or higher and other sun protection measures including: • Limit time in the sun, especially from10 a.m.-2 p.m. • Wear long-sleeved shirts, pants, hats, and sunglasses • Children under 6 months: Ask a physician
Warnings
For external use only
Frequently asked questions
What is MEDULTIMA ADVENTURE SUNSCREEN used for?
helps prevent sunburn
Who makes MEDULTIMA ADVENTURE SUNSCREEN?
Guangzhou Tata Biotechnology Co., Ltd. is the labeler of record for MEDULTIMA ADVENTURE SUNSCREEN.
What form does MEDULTIMA ADVENTURE SUNSCREEN 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 MEDULTIMA ADVENTURE SUNSCREEN 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.
Has MEDULTIMA ADVENTURE SUNSCREEN 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.