FDA.reportPublic FDA data

spf30 mineral sunscreen mousse

Manufacturer
Aopline Health Industry Technology (Guangzhou) Co., Ltd.
Effective date
2025-08-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:11:53

Label at a glance#

Productspf30 mineral sunscreen mousse
Active ingredientZINC OXIDE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide（nano）15%

INACTIVE INGREDIENT SECTION

Water
Butane
Isobutane
Propane
Glycerin
PEG-17 Dimethicone
Propylene Glycol
Stearic Acid
Palmitic Acid
Triethanolamine
Glyceryl Stearate
PEG-100 Stearate
PEG-7 Glyceryl Cocoate
Jojoba Wax PEG-120 Esters
Cetearyl Alcohol
Hydroxyacetophenone
1,2-Hexanediol
Butylene Glycol
Gentiana Scabra Root Extract
Dipotassium Glycyrrhizate
Sodium Hyaluronate
Disodium EDTA
Hibiscus Esculentus Fruit Extract

OTC - PURPOSE SECTION

Helps prevent sunbum, if used as directed withother sun protection measures (see Direciions), decreasesthe risk of skin cancer and eary aging caused by the sun

WARNINGS SECTION

For extemal use onl,.
Do not use on damaged or broken skn,
When using this product keep out of cyes, Rinse withwater to remowe,
Siop use and ask a doctor if rash cccurs.Keep out of reach of children, lf product is swalkawed, getmedical help or contact a Potson Conirol Centre right away.Wlay stain some fabrics.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

Apply liberaly 15 minues before sunexposure,

Reapply: After 80 minutes of swimming orsseating,

lmmedabely after touel drying.. At leastevery 2 hours,

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of children to use it

INDICATIONS & USAGE SECTION

1.Avoid contact with eyes. lf it gets into eye accidentally, please rinse with clean water 2. This product is pressure pocked. Do not impact. Keep away from fire out of reach of children.3. Due to differences in human constitution, this product may have adheres reactions an a few people you feel uncontactable, please stop using
4. Do not puncture the product and empty cans or show then into fire.5. Please store in a dry and place below40℃, avoid high temperature and direct sunlight,、

DOSAGE & ADMINISTRATION SECTION

Directions: Apply liberaly 15 minues before sunexposure, e Reapply: After 80 minutes of swimming or seating,. lmmedabely after touel drying.. At leastevery 2 hours,

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82723-031-01spf30 mineral sunscreen mousse166 mL in 1 BOTTLE, SPRAYSPRAY1661

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82723-03182723-031-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BUTANE6LV4FOR43RIACT
PROPANET75W9911L6IACT
GLYCERINPDC6A3C0OXIACT
DIPOTASSIUM GLYCYRRHIZATECA2Y0FE3FXIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
PALMITIC ACID2V16EO95H1IACT
PEG-12 DIMETHICONEZEL54N6W95IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PEG-100 STEARATEYD01N1999RIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
SODIUM HYALURONATEYSE9PPT4THIACT
EDETATE DISODIUM7FLD91C86KIACT
ZINC OXIDESOI2LOH54ZACTIB
ISOBUTANEBXR49TP611IACT
STEARIC ACID4ELV7Z65APIACT
TROLAMINE9O3K93S3TKIACT
GLYCERYL STEARATE230OU9XXE4IACT
PEG-7 GLYCERYL COCOATEVNX7251543IACT
HYDROGENATED JOJOBA OIL/JOJOBA OIL, RANDOMIZED (IODINE VALUE 64-70)96YYQ5TK1KIACT
CETEARYL ALCOHOL2DMT128M1SIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
GENTIANA SCABRA ROOTGXZ33VNT92IACT
OKRA51ME2L7STLIACT

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
3d5613e0-9948-be1e-e063-6394a90a341f3d5613e0-9947-be1e-e063-6394a90a341f2025-08-27WarningsExact identifier
spl id: 3d5613e0-9948-be1e-e063-6394a90a341f
spl set id: 3d5613e0-9947-be1e-e063-6394a90a341f

Reported adverse events (FAERS/openFDA)#

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