Mineralized Loose Powder SPF 15

Manufacturer
Modern Beauty Limited | Guangzhou Zilin Cosmetic Co., Ltd.
Effective date
2015-12-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:44:21

Label at a glance#

ProductMineralized Loose Powder SPF 15
Active ingredientTITANIUM DIOXIDE, OCTINOXATE
Label structure11 sections

Dosage and administration

•apply liberally 15 minutes before sun exposure •reapply:    •after 40 minutes of swimming or sweating    •immediately after towel drying    •at least every 2 hours •Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:   ...

Storage and handling

Protect this product from excessive heat and direct sun

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 7.12%

Ethylhexyl Methoxycinnamate 2%

Purpose

OTC - PURPOSE SECTION

Sunscreen

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact Poison Centre right away.

Use

INDICATIONS & USAGE SECTION

•helps prevent sunburn
•if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

WARNINGS SECTION

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes.

Remove with water and mild cleanser

Stop use and ask a doctor if rash occurs.

Directions

DOSAGE & ADMINISTRATION SECTION

•apply liberally 15 minutes before sun exposure
•reapply:
   •after 40 minutes of swimming or sweating
   •immediately after towel drying
   •at least every 2 hours
•Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
   •limit time in the sun, especially from 10 a.m-2 p.m
   •Wear long-sleeved shirts, pants, hats and sunglasses
•children under 6 months of age: Ask a doctor.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: MICA, MAGNESIUM MYRISTATE, NYLON-12, SILICA, DIMETHICONE, SIMMONDSIA CHINENSIS(JOJOBA)SEED OIL, BORON NITRIDE, PHENOXYETHANOL, METHYLPARABEN, BUTYLPARABEN, ETHYLPARABEN, PROPYLPARABEN, ISOBUTYLPARABEN, BHT, MAY CONTAIN:[YELLOW IRON OXIDE(CI77492), RED IRON OXIDE(CI77491), BLACK IRON OXIDE(CI77499), FD&C RED 40 AL LAKE(CI16035), FD&C YELLOW 5 AL LAKE(CI19140:1), FD&C YELLOW 6 AL LAKE(CI15985:1)]

Other Information

STORAGE AND HANDLING SECTION

Protect this product from excessive heat and direct sun

Questions

OTC - QUESTIONS SECTION

Call toll free 1-877-438-1120

SPL UNCLASSIFIED SECTION

FORMULATED FOR PROFESSIONAL APPLICATION

THIS CARTON IS MADE FROM RECYCLED PAPER

CRUELTY FREE - THIS PRODUCT HAS NEVER BEEN TESTED ON ANIMALS.

MADE IN CHINA

MODERN BASIC,BURNABY CANADA/GARDEN GROVE CA.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

mineralmineral

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69349-102-332020-01-31C16284748780-19d75b9d0-7ff6-f424-e053-dadaa90a57ceMINERALIZED LOOSE POWDER SPF 15

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69349-102-33Mineralized Loose Powder SPF 1515 g in 1 CONTAINERPOWDER151
69349-102-33Mineralized Loose Powder SPF 151 in 1 CARTONPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69349-102MINERALIZED LOOSE POWDER SPF 15 (TITANIUM DIOXIDE, ETHYLHEXYL METHOXYCINNAMATE) POWDER [MODERN BEAUTY LIMITED]1Legacy NDC, 2 package rows20151214_59173171-1d9d-434a-ad8b-40ba88fc707a.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69349-10269349-102-33

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
f14dd99d-a99a-481e-b496-aa22e273555759173171-1d9d-434a-ad8b-40ba88fc707a2015-12-05WarningsExact identifier
spl id: f14dd99d-a99a-481e-b496-aa22e2735557
spl set id: 59173171-1d9d-434a-ad8b-40ba88fc707a

Reported adverse events (FAERS/openFDA)#

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