FACE SPF 47 SETTING- face spf 47 setting spray spray

FACE SPF 47 SETTING by

Drug Labeling and Warnings

FACE SPF 47 SETTING by is a Otc medication manufactured, distributed, or labeled by Aopline Biotechnology (Guangzhou) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Homosalate 8.0%

Octisalate 5.0%

Octocrylene 3.0%

Avobenzone 3.0%

PURPOSE

Sunscreen

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

WARNINGS

For External Use Only.

Do not use on damaged or broken skin.

Keep out of reach of children.

Keep out of eyes. Rinse with water to remove.

Stop use and ask a physician if rash occurs.

Keep out of reach of children . If product is swallowed, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION

Apply to face 15 minutes before sun exposure.

Reapply every 2 hours.

INACTIVE INGREDIENT

Vitamin E, Vitamin C, Hyaluronic Acid, Niacinamide, Peppermint Extract, Eucalyptus Extract, Sunflower Seed Oil, Tea Tree Extract, Alcohol, Cyclohexasiloxane, Cyclopentasiloxane, Ethylhexyl Palmitate

INDICATIONS & USAGE

Helps prevent sunburn. If used as directed with other sun protection measures, decrease the risk of skin cancer and early skin aging caused by sun.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FACE SPF 47 SETTING 
face spf 47 setting spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87283-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	3 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	8 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
ALCOHOL (UNII: 3K9958V90M)
HYALURONIC ACID (UNII: S270N0TRQY)
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
SUNFLOWER OIL (UNII: 3W1JG795YI)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
NIACINAMIDE (UNII: 25X51I8RD4)
PEPPERMINT (UNII: V95R5KMY2B)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
ASCORBIC ACID (UNII: PQ6CK8PD0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87283-001-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/08/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/08/2026

Labeler - Aopline Biotechnology (Guangzhou) Co., Ltd. (514879104)

Registrant - Aopline Biotechnology (Guangzhou) Co., Ltd. (514879104)