FDA.reportPublic FDA data

sunscreen

Manufacturer
Mingyu (guangdong) Cosmetics Technology Co., Ltd
Effective date
2025-09-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:13:39

Label at a glance#

Productsunscreen
Active ingredientTITANIUM DIOXIDE, ETHYLHEXYL METHOXYCINNAMATE
Label structure8 sections

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

WATER
SACCHAROMYCES FERMENT FILTRATE
DIPROPYLENE GLYCOL
GLYCERIN
C12-15 ALKYL BENZOATE
CAPRYLYL METHICONE
CYCLOPENTASILOXANE
POLYMETHYLSILSESQUIOXANE
METHYLENE BIS-BENZOTRIAZOLYL
TETRAMETHYLBUTYLPHENOL(NANO)
BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL
TRIAZINE
DIETHYLAMINO HYDROXYBENZOYL HEXYL
BENZOATE
CYCLOHEXASILOXANE
C20-22 ALKYL PHOSPHATE
POTASSIUM CETYL PHOSPHATE
HYDROXYACETOPHENONE
SILICA
C20-22 ALCOHOLS
POLYGLYCERYL-10 MYRISTATE
CETEARYL ALCOHOL
POLYHYDROXYSTEARIC ACID
TOCOPHERYL ACETATE
CHLORPHENESIN
DECYL GLUCOSIDE
POLYACRYLATE CROSSPOLYMER-6
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER
SODIUM ACRYLATE/SODIUM
ACRYLOYLDIMETHYL TAURATE COPOLYMER
POTASSIUM HYDROXIDE
DISODIUM EDTA
BISABOLOL
DIMETHICONE
ISOHEXADECANE
POLYSORBATE 80
PROPYLENE GLYCOL
SODIUM HYALURONATE CROSSPOLYMER
SODIUM HYALURONATE
SORBITAN OLEATE
XANTHAN GUM
PHENOXYETHANOL
VIOLA YEDOENSIS EXTRACT
PAEONIA LACTIFLORA ROOT EXTRACT
TARAXACUM OFFICINALE (DANDELION)
RHIZOME/ROOT EXTRACT
CHAMOMILLA RECUTITA (MATRICARIA)
FLOWER EXTRACT
BHT
1,2-HEXANEDIOL
LONICERA JAPONICA (HONEYSUCKLE) FLOWER EXTRACT
MALVA SYLVESTRIS (MALLOW) FLOWER
EXTRACT
HYDROLYZED SODIUM HYALURONATE
SODIUM ACETYLATED HYALURONATE
HYALURONIC ACID
HYDROLYZED GLYCOSAMINOGLYCANS
ZINGIBER OFFICINALE (GINGER) ROOT
EXTRACT
ETHYLHEXYLGLYCERIN
HYDROXYPROPYLTRIMONIUM HYALURONATE
ALOE BARBADENSIS LEAF JUICE

OTC - ACTIVE INGREDIENT SECTION

ETHYLHEXYL METHOXYCINNAMATE 7.5%

TITANIUM DIOXIDE(NANO) 4%

DOSAGE & ADMINISTRATION SECTION


USAGE：For daytime use, apply an appropriate amount evenly to the face and body.

WARNINGS SECTION


PRECAUTIONS:
Do not use for food purposes.Do not use on broken skin; avoid contact with eyes.
If product gets into eyes, rinse immediately with plenty of water. Discontinue use if discomfort occurs.

INDICATIONS & USAGE SECTION


FUNCTION:
Blocks UV rays. protects against sun damage, moisturizes and nourishes,
feels light and breathable, and nourishes and beautifies the skin.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of eyes: In case of contact with eyes, please fush thoroughly with water.

OTC - PURPOSE SECTION

Sun Protection

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label imageLabel image

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87091-001-01sunscreen50 g in 1 BOTTLELOTION501

Products#

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

DailyMed product names page 1 of 2 · 56 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87091-00187091-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 54 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAPRYLYL METHICONEQ95M2P1KJLIACT
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)59Z907ZB69IACT
METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL8NT850T0YSIACT
LONICERA JAPONICA FLOWER4465L2WS4YIACT
GINGERC5529G5JPQIACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW)1DXE3F3OZXIACT
AQUA059QF0KO0RIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
CYCLOHEXASILOXANEXHK3U310BAIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATEANQ870JD20IACT
MALVA SYLVESTRIS WHOLEI01732476CIACT
HYDROLYZED GLYCOSAMINOGLYCANS (BOVINE; 50000 MW)997385V0VVIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
ETHYLHEXYL METHOXYCINNAMATE4Y5P7MUD51ACTIB
DIPROPYLENE GLYCOLE107L85C40IACT
SACCHAROMYCES LYSATER85W246Z1CIACT
VIOLA PHILIPPICA WHOLEO176VC3N54IACT
TARAXACUM OFFICINALE (DANDELION) ROOT9DE5YCO0RUIACT
POLYACRYLATE CROSSPOLYMER-6Q7UI015FF9IACT
DIMETHICONE92RU3N3Y1OIACT
SORBITAN OLEATE06XEA2VD56IACT
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER788QAG3W8AIACT
SODIUM HYALURONATEYSE9PPT4THIACT
XANTHAN GUMTTV12P4NEEIACT
CHAMOMILEFGL3685T2XIACT
BHT1P9D0Z171KIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
SODIUM ACETYLATED HYALURONATEWN66R7GL93IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT
BISABOLOL24WE03BX2TIACT
CHLORPHENESINI670DAL4SZIACT
ISOHEXADECANE918X1OUF1EIACT
HYALURONIC ACIDS270N0TRQYIACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)8Z5ZAL5H3VIACT
PAEONIA LACTIFLORA ROOT3Z3866YW6PIACT

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
sunscreenTITANIUM DIOXIDE(NANO)Mingyu (guangdong) Cosmetics Technology Co., Ltd3e6fe9f3-486b-bba7-e063-6294a90adf372025-09-10WarningsExact identifier
ndc (package): 87091-001-01
ndc (product): 87091-001
ndc11 (package): 87091000101
spl id: 3e6fe9f3-486c-bba7-e063-6294a90adf37
spl set id: 3e6fe9f3-486b-bba7-e063-6294a90adf37

Reported adverse events (FAERS/openFDA)#

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