Mineral Sunscreen SPF 50
Mineral Sunscreen SPF 50 is an FDA drug label for the active ingredient MINERAL SUNSCREEN manufactured by ALAINA HEALTHCARE PRIVATE LIMITED 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 20260617.
- Generic name
- MINERAL SUNSCREEN
- Manufacturer
- ALAINA HEALTHCARE PRIVATE LIMITED
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 73492-720
- Application
- M020
- Label effective
- 20260617
About this product
Mineral Sunscreen SPF 50 is an FDA-registered drug product whose active ingredient is MINERAL SUNSCREEN. It is labelled by ALAINA HEALTHCARE PRIVATE LIMITED taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 73492-720, application M020, label effective 20260617. It is one of 4 FDA drug label records sharing the active ingredient MINERAL 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 MINERAL SUNSCREEN 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 Apply generously and evenly 15 minutes before sun exposure Reapply: after 40 minutes of swimming or sweating immediately after towel drying 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 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: 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 product is swallowed, get medical help or contact a Poison Control Center right away.
More products with the same ingredient
MINERAL SUNSCREENHow products containing MINERAL SUNSCREEN compare
FDA lists 4 drug label records with MINERAL 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 |
|---|---|---|---|
| — | — | ALAINA HEALTHCARE PRIVATE LIMITED | 1 |
| — | — | Guangzhou Origin Beauty Cosmetics Co., Ltd. | 1 |
| — | — | PANERGYTEK USA INC | 1 |
| — | — | doTERRA International, LLC | 1 |
| — | — | — | — |
Recall and safety notices
5 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-0194-2026 | Elixir by Coco March Tinted Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz (62g) per bottle, Distributed by: VitaTienda Co U.S.A., San Juan, PR 00646. NDC: 35192-050-17, UPC 6 7229 99913 8 | CA BOTANA International, Inc. | Class II | Ongoing | 20251203 |
| D-0192-2026 | Sugared+Bronzed Tinted Mineral Sunscreen SPF 50, Zinc Oxide 21%, Net WT 3.3 OZ (93 G) per tube, Dist. By: Sugared+Bronzed, 929 Montana Ave, Santa Monica, CA 90403. NDC: 35192-055-18, UPC 8 50047 92223 6 | CA BOTANA International, Inc. | Class II | Ongoing | 20251203 |
| D-0183-2026 | Doctor. D. Schwab Mineral Sunscreen SPF 50, Zinc Oxide 21%, 4 oz./ 113.4 g per tube, Manufactured by CA Botana, San Diego, CA 92123. NDC: 35192-042-02 | CA BOTANA International, Inc. | Class II | Ongoing | 20251203 |
| D-0193-2026 | Elixir by Coco March Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz (62g) per bottle, Distributed by: VitaTienda Co U.S.A., San Juan, PR 00646. NDC: 35192-048-17, UPC 8 10145 82007 0 | CA BOTANA International, Inc. | Class II | Ongoing | 20251203 |
| D-0190-2026 | Gabriel Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz, Net 61 g per tube, Dist. By: Gabriel Cosmetics, Inc., Redmond, WA USA 98052, NDC: 35192-044-01, UPC 7 07060 9592 1 | CA BOTANA International, Inc. | Class II | Ongoing | 20251203 |
Frequently asked questions
What is Mineral Sunscreen SPF 50 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 Mineral Sunscreen SPF 50?
ALAINA HEALTHCARE PRIVATE LIMITED is the labeler of record for Mineral Sunscreen SPF 50. 4 FDA label records share the active ingredient MINERAL 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 Mineral Sunscreen SPF 50 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 Mineral Sunscreen SPF 50 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 MINERAL SUNSCREEN?
Yes. 4 FDA drug label records list MINERAL 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 Mineral Sunscreen SPF 50 been recalled?
5 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.