X-Treme Cream Propolis Sunscreen SPF 45
X-Treme Cream Propolis Sunscreen SPF 45 is an FDA drug label for the active ingredient X-TREME CREAM manufactured by Epicuren Discovery 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 20260714.
- Generic name
- X-TREME CREAM
- Manufacturer
- Epicuren Discovery
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 84378-101
- Application
- M020
- Label effective
- 20260714
About this product
X-Treme Cream Propolis Sunscreen SPF 45 is an FDA-registered drug product whose active ingredient is X-TREME CREAM. It is labelled by Epicuren Discovery taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 84378-101, application M020, label effective 20260714. 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.
Active ingredients
Indications & Usage
Indications and Uses
Dosage & Administration
Dosage
Warnings
Warnings Section
Frequently asked questions
What is X-Treme Cream Propolis Sunscreen SPF 45 used for?
Indications and Uses
Who makes X-Treme Cream Propolis Sunscreen SPF 45?
Epicuren Discovery is the labeler of record for X-Treme Cream Propolis Sunscreen SPF 45.
What form does X-Treme Cream Propolis Sunscreen SPF 45 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 X-Treme Cream Propolis Sunscreen SPF 45 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 X-Treme Cream Propolis Sunscreen SPF 45 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.