FDA.reportPublic FDA data

IQQU Advance Sunscreen

Manufacturer
IQQU USA Co.
Effective date
2010-02-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:23:33

Label at a glance#

ProductIQQU Advance Sunscreen
Active ingredientDIMETHICONE, AVOBENZONE, TITANIUM DIOXIDE, OCTINOXATE
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 35 UVA/UVB

Active Ingredient

DESCRIPTION SECTION

Dimethicone, Butyl Methoxydibenzoylmethane, Titanium Dioxide, Octyl Methoxycinnamate.

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.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Isononyl Isonanonate, Glyceryl Stearate, Cyclopentasiloxane (and) Dimethicone, Cyclopentasiloxane (and) C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Talcum


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

Package Label – 30 mL 

IQQU Advance Sunscreen

SPF 35 UVA/UVB

30 mL /1.01 oz

Principal Display Panel - 30 mL /1.01 ozPrincipal Display Panel - 30 mL /1.01 oz

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DIMETHICONE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50403-999-922019-10-21C16284748780-1956f9ecf-ccff-621f-e053-dbdaa90a74adAdvance Sunscreen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50403-999-92IQQU Advance Sunscreen30 mL in 1 TUBELOTION303
50403-999-92IQQU Advance Sunscreen1 in 1 CARTONLOTION13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50403-999IQQU ADVANCE SUNSCREEN (DIMETHICONE AND BUTYL METHOXYDIBENZOYLMETHANE AND TITANIUM DIOXIDE AND OCTYL METHOXYCINNAMATE) LOTION [IQQU USA CO.]3Legacy NDC, 2 package rows20100205_e35234bf-ee75-4cb6-8984-e5ed4a293696.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX3
DIMETHICONEACTIVE INGREDIENT92RU3N3Y1O3
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD513
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP3
AVOBENZONEACTIVE MOIETYG63QQF2NOX3
DIMETHICONEACTIVE MOIETY92RU3N3Y1O3
OCTINOXATEACTIVE MOIETY4Y5P7MUD513
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP3
GLYCERYL MONOSTEARATEINACTIVE INGREDIENT230OU9XXE43

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50403-99950403-999-92

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE92RU3N3Y1OACTIB
AVOBENZONEG63QQF2NOXACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
OCTINOXATE4Y5P7MUD51ACTIB
GLYCERYL MONOSTEARATE230OU9XXE4IACT

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 · 21 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4EMULSION / ORALNAExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4SUSPENSION / OPHTHALMIC0.5 %w/vExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4GRANULE, FOR SUSPENSION / ORAL4 mgExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4TABLET / ORAL33.34 mgExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4LIQUID / TOPICAL1 %w/wExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4CREAM / VAGINAL140 mgExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4AEROSOL, FOAM / TOPICAL3.27 %w/wExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4OINTMENT / TOPICAL5 %w/wExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4CAPSULE, DELAYED RELEASE / ORAL15 mgExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4LOTION / TOPICAL177 mgExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4TABLET / SUBLINGUAL1.23 mgExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL23 mgExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4TABLET, EXTENDED RELEASE / ORAL529 mgExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4CREAM / TOPICAL836 mgExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4TABLET, DELAYED RELEASE / ORAL6 mgExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4TABLET, CHEWABLE / ORAL1 mgExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4AEROSOL, FOAM / VAGINAL3 %w/wExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4SUSPENSION / AURICULAR (OTIC)0.5 %w/vExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4SUPPOSITORY / RECTAL35 mgExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4CAPSULE / ORAL13.75 mgExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERYL MONOSTEARATEGLYCERYL MONOSTEARATE230OU9XXE4CAPSULE, EXTENDED RELEASE / ORAL32.4 mgExact identifier — unii candidate
21 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
2083b860-64a8-4ea5-b56f-5af21f82bb2ae35234bf-ee75-4cb6-8984-e5ed4a2936962010-02-07WarningsExact identifier
spl id: 2083b860-64a8-4ea5-b56f-5af21f82bb2a
spl set id: e35234bf-ee75-4cb6-8984-e5ed4a293696

Reported adverse events (FAERS/openFDA)#

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