MENOW SUNSCREEN

Manufacturer
SHANTOU QIWEI INDUSTRY CO.,LTD
Effective date
2025-01-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:53:13

Label at a glance#

ProductMENOW SUNSCREEN
Active ingredientBIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, ZINC OXIDE, ETHYLHEXYL METHOXYCINNAMATE, TITANIUM DIOXIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: ETHYLHEXYL METHOXYCINNAMATE(5.83874g/100g), BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE(0.772g/100g), ZINC OXIDE(11.89646/100g), TITANIUM DIOXIDE(8.02712g/100g)

OTC - PURPOSE SECTION

Use to Absorbs UVA and UVB rays to protect skin from UV rays.Prevent sunburn, tanning, and skin photoaging

INDICATIONS & USAGE SECTION

Indications & usage section:SUNSCREEN PRESSED POWDER,SETTING MAKEUP WHILE PROTECTING AGAINST UVA/UVB

WARNINGS SECTION

Warnings:

1.IF YOU HAVE SENSITIVE SKIN, PLEASE TRY IT LOCALLY FIRST ANDUSE IT AFTER NO DISCOMFORT;

2.DISCONTINUE USE IMMEDIATELY IF YOU FEELUNWELL AFTER USE;

3.KEEP OUT OF REACH OF YOUNG CHILDREN TO AVOID ACCI.DENTAL INGESTION, NOT BE USED FOR CHILDREN UNDER 3 YEARS OF AGE.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS:

SIMPLY DAB AN APPROPRIATE AMOUNT OF POWDER WITH THE PUFF AND APPLY TO THE FACE FROM THE INSIDE OUT BY PATTING AND PRESSING EVENLY.

INACTIVE INGREDIENT SECTION

Inactive ingredients:

TALC, MICA, SILICA, METHYL METHACRYLATE CROSSPOLYMER, BORON NITRIDE, MAGNESIUM STEARATE, TRIETHOXYCAPRYLYLSILANE, ETHYLHEXYL PALMITATE, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, DIMETHICONE, PHENOXYETHANOL, ALUMINUM HYDROXIDE, STEARIC ACID, CI 77492, PORTULACA OLERACEA EXTRACT, ARGANIA SPINOSA KERNEL OIL, TOCOPHERYL ACETATE, POLYHYDROXYSTEARIC ACID, CI 77491, PENTAERYTHRITYL TETRA-DI-t-BUTYL HYDROXYHYDROCINNAMATE, GLYCYRRHIZIC ACID, LIMNANTHES ALBA (MEADOWFOAM) SEED OIL, MACADAMIA TERNIFOLIA SEED OIL, ECTOIN, AQUA, CI 77499, BISABOLOL, GLYCERIN, OENOTHERA BIENNIS (EVENING PRIMROSE) SEED EXTRACT, CRITHMUM MARITIMUM EXTRACT, BHT, SODIUM CHLORIDE, SODIUM SULFATE, ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT, 1,2-HEXANEDIOL, HYDROXYACETOPHENONE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF YOUNG CHILDREN TO AVOID ACCIDENTAL INGESTION,NOT BE USED FOR CHILDREN UNDER 3YEARS OF AGE.

OTHER SAFETY INFORMATION

PLEASE KEEP IN A DRY PLACE AT ROOM TEMPERATURE AND AVOID DIR-ECT SUNLIGHT.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

See label LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85138-101-01MENOW SUNSCREEN9 g in 1 BOXPOWDER91
85138-101-02MENOW SUNSCREEN1 in 1 BOXPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85138-101MENOW SUNSCREEN (ETHYLHEXYL METHOXYCINNAMATE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, ZINC OXIDE, TITANIUM DIOXIDE) POWDER [SHANTOU QIWEI INDUSTRY CO.,LTD]12 package rows20250121_2be1dfce-1881-aab3-e063-6394a90ac464.zip

Products#

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

DailyMed product names page 1 of 2 · 42 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85138-10185138-101-01, 85138-101-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 40 matching rows.

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
2be1dfce-1882-aab3-e063-6394a90ac4642be1dfce-1881-aab3-e063-6394a90ac4642025-01-17WarningsExact identifier
spl id: 2be1dfce-1882-aab3-e063-6394a90ac464
spl set id: 2be1dfce-1881-aab3-e063-6394a90ac464

Reported adverse events (FAERS/openFDA)#

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