FDA.reportPublic FDA data

Biopo Facial Mineral Sunscreen- Tinted SPF 40

Manufacturer
MERRYLAZ USA LLC
Effective date
2024-12-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:47:25

Label at a glance#

ProductBiopo Facial Mineral Sunscreen- Tinted SPF 40
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure12 sections

Dosage and administration

1.Apply generous amount to skin 15 minutes before sun exposure. 2. Wait 10-15 minutes for sunscreen to be fully absorbed. 3. Reapply after 80 minutes of swimming or sweating. 4. Apply after immediately towel drying.

Storage and handling

Sunscreen may stain some fabrics.Protect this product from direct exposure to sunlight or excessive heat.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 5.22%

Titanium Dioxide 3%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

Helps prevent sunburn. Decreases the signs of early skin aging and risk of skin disease caused by the
sun.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use on damaged skin.

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes. If contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Discontinue use if redness or irritation occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

1.Apply generous amount to skin 15 minutes before sun exposure.
2. Wait 10-15 minutes for sunscreen to be fully absorbed.
3. Reapply after 80 minutes of swimming or sweating.
4. Apply after immediately towel drying.

Other information

STORAGE AND HANDLING SECTION

Sunscreen may stain some fabrics.Protect this product from direct exposure to sunlight or
excessive heat.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alumina, Cyclopentasiloxane, Dimethicone, Dimethicone/Vinyl Dimethicone Crosspolymer,
Dimethicone Crosspolymer, Hydrogenated Coconut Oil, Jojoba Esters, PhenyI Trimethicone, Silica,
Stearic Acid, Tetrahexyldecyl Ascorbate, Tocopheryl Acetate, Triethoxycaprylylsilane,
CI 77492, CI 77491, CI 77499.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84874-002BIOPO FACIAL MINERAL SUNSCREEN- TINTED SPF 40 CREAM [MERRYLAZ USA LLC]1Unmatched20241207_2844ebc9-b734-0f9e-e063-6394a90a615d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84874-00284874-002-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
SILICAETJ7Z6XBU4IACT
STEARIC ACID4ELV7Z65APIACT
CI 77499XM0M87F357IACT
CI 77492EX438O2MRTIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
DIMETHICONE92RU3N3Y1OIACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE)H895X08VNQIACT
DIMETHICONE CROSSPOLYMERUF7620L1W6IACT
HYDROGENATED COCONUT OILJY81OXM1OMIACT
JOJOBA OIL, RANDOMIZED7F0EV20QYLIACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
ZINC OXIDESOI2LOH54ZACTIB
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
CI 774911K09F3G675IACT
TETRAHEXYLDECYL ASCORBATE9LBV3F07AZIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3b349d45-6901-61d9-e063-6394a90aeeed2844ebc9-b734-0f9e-e063-6394a90a615d2025-07-31WarningsExact identifier
spl set id: 2844ebc9-b734-0f9e-e063-6394a90a615d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.