BIOPO FACIAL MINERAL SUNSCREEN- TINTED SPF 40 cream

Biopo Facial Mineral Sunscreen- Tinted SPF 40 by

Drug Labeling and Warnings

Biopo Facial Mineral Sunscreen- Tinted SPF 40 by is a Otc medication manufactured, distributed, or labeled by Guangzhou Ariel Biotech Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Zinc Oxide 5.22%
Titanium Dioxide 3%

Purpose

Sunscreen

Use

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

Warnings

For external use only.
Store at room temperature.
Discontinue use if redness or irritation occurs.
Keep out of reach of children.
Rinse with water to remove.
If swallowed get medical help and contact a poison
control center right away.
Do not use on damaged skin.
When using this product, avoid contact with eyes. If
contact occurs, rinse thoroughly with water.

Do not use

Do not use on damaged skin.

WHEN USING

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

STOP USE

Discontinue use if redness or irritation occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Directions

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

Sunsceen may stain some fbric.Protect this
product from direct exposure to sunlight or
excessive heat.

Inactive ingredients

Alumina, Cyclopentasiloxane, Dimethicone,
Dimethicone/VinyI 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

INGREDIENTS AND APPEARANCE

BIOPO FACIAL MINERAL SUNSCREEN- TINTED SPF 40 
biopo facial mineral sunscreen- tinted spf 40 cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84148-015
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	5.22 g  in 100 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
STEARIC ACID (UNII: 4ELV7Z65AP)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CI 77492 (UNII: EX438O2MRT)
CI 77499 (UNII: XM0M87F357)
SILICA (UNII: ETJ7Z6XBU4)
CI 77491 (UNII: 1K09F3G675)
DIMETHICONE (UNII: 92RU3N3Y1O)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
DIMETHICONE CROSSPOLYMER (UNII: UF7620L1W6)
HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)
HYDROLYZED JOJOBA ESTERS (UNII: UDR641JW8W)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84148-015-01	50 g in 1 BOTTLE; Type 0: Not a Combination Product	11/04/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/04/2025

Labeler - Guangzhou Ariel Biotech Co., Ltd. (402818771)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Ariel Biotech Co., Ltd.		402818771	manufacture(84148-015)