IQQU Advanced Sunscreen SPF 50

Manufacturer
IQQU USA Co. | JUNE LABORATORIES COMPANY LIMITED
Effective date
2010-12-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:26:29

Label at a glance#

ProductIQQU Advanced Sunscreen SPF 50
Active ingredientOCTINOXATE, JOJOBA OIL, TITANIUM DIOXIDE, .ALPHA.-TOCOPHEROL ACETATE, D-, LYCOPENE, SACCHARIDE ISOMERATE
Label structure6 sections

Dosage and administration

Advance formula, use a small amount only. Apply evenly over clean skin until fully absorbed. Apply as needed before sun exposure. Keep the sunscreen tube away from direct sunlight to preserve its efficiency.      

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

IQQU 
Advance Sunscreen 
SPF 50 UVA/UVB

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Octyl Methoxycinnamate, Simmondsia Chinensis (jojoba) Seed oil, Titanium Dioxide, Tocopheryl Acetate, Saccharide Isomerate, Lycopene Extract

This sunscreen is special.

OTC - PURPOSE SECTION

It has a non greasy, non oily formula. It feels like nothing when you apply it on and provides maximum SPF 50 UVA/UVB protection. It can be applied over makeup, making this a cosmetic sunscreen.

Non-Comedogenic. No Fragrance. Paraben Free

This product is for you if

INDICATIONS & USAGE SECTION

You want an advanced sun protection for your skin. You want a non-greasy, non-sticky, smooth velvety sunscreen. You want to have a silky complexion. You want to fade your brown spots. you want a sunscreen that is makeup friendly. You want a sunscreen that does not run easily.

Directions

DOSAGE & ADMINISTRATION SECTION

Advance formula, use a small amount only. Apply evenly over clean skin until fully absorbed. Apply as needed before sun exposure.

Keep the sunscreen tube away from direct sunlight to preserve its efficiency.      

Warnings

WARNINGS SECTION

For external use only. Avoid contact with the eyes. Discontinue use if signs of irritation occurs.

Keep out of children’s reach.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane (and) Dimethicone Cross Polymer, Octocrylene, Cetyl Dimethicone, Talcum, Ironoxides C.I. 77491, C.I. 77492


Manufactured by: June Laboratories Co., Ltd. 
1014 Soi Wat Channai, Sathupradit Rd, 
Bangkok 10120 Thailand.

Made in Thailand

www.iqqubeauty.com      

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IQQU Advance Sunscreen

SPF 50 UVA/UVB

30 mL /1.01 oz

PRINCIPAL DISPLAY PANEL IQQU Advance Sunscreen SPF 50 UVA/UVB 30 mL /1.01 ozPRINCIPAL DISPLAY PANEL IQQU Advance Sunscreen SPF 50 UVA/UVB 30 mL /1.01 oz

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50403-050-302019-10-29C16284748780-1960f7f55-ca3d-8e05-e053-dbdaa90a074aAdvanced Sunscreen SPF50

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50403-050-30IQQU Advanced Sunscreen SPF 501 in 1 CARTONLOTION12
50403-050-30IQQU Advanced Sunscreen SPF 5030 g in 1 TUBELOTION302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50403-050IQQU ADVANCED SUNSCREEN SPF 50 (OCTYL METHOXYCINNAMATE AND SIMMONDSIA CHINENSIS SEED OIL AND TITANIUM DIOXIDE AND TOCOPHERYL ACETATE) LOTION [IQQU USA CO.]2Legacy NDC, 2 package rows20101203_d71b2d4b-a5db-4f69-a194-626466338efc.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
.ALPHA.-TOCOPHEROL ACETATE, D-ACTIVE INGREDIENTA7E6112E4N2
JOJOBA OILACTIVE INGREDIENT724GKU717M2
LYCOPENEACTIVE INGREDIENTSB0N2N0WV62
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD512
SACCHARIDE ISOMERATEACTIVE INGREDIENTW8K377W98I2
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP2
.ALPHA.-TOCOPHEROL ACETATE, D-ACTIVE MOIETYA7E6112E4N2
JOJOBA OILACTIVE MOIETY724GKU717M2
LYCOPENEACTIVE MOIETYSB0N2N0WV62
OCTINOXATEACTIVE MOIETY4Y5P7MUD512
SACCHARIDE ISOMERATEACTIVE MOIETYW8K377W98I2
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP2
CYCLOMETHICONE 5INACTIVE INGREDIENT0THT5PCI0R2
OCTOCRYLENEINACTIVE INGREDIENT5A68WGF6WM2

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50403-05050403-050-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
CYCLOMETHICONE 5CYCLOMETHICONE 50THT5PCI0RCREAM, AUGMENTED / TOPICAL260 mgExact identifier — unii candidate
3 equally ranked IID candidates
CYCLOMETHICONE 5CYCLOMETHICONE 50THT5PCI0RAEROSOL / TOPICAL2.5 %w/wExact identifier — unii candidate
3 equally ranked IID candidates
CYCLOMETHICONE 5CYCLOMETHICONE 50THT5PCI0RAEROSOL, FOAM / TOPICAL144 mgExact identifier — unii candidate
3 equally ranked IID candidates

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
c64d5251-a899-4b64-9d6d-d0d285bbe92ed71b2d4b-a5db-4f69-a194-626466338efc2010-12-03WarningsExact identifier
spl id: c64d5251-a899-4b64-9d6d-d0d285bbe92e
spl set id: d71b2d4b-a5db-4f69-a194-626466338efc

Reported adverse events (FAERS/openFDA)#

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