ULTIMATE AQUA BLANC PROTECTIVE

Manufacturer
Racinne (Hong Kong) Limited
Effective date
2014-06-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:39:36

Label at a glance#

ProductULTIMATE AQUA BLANC PROTECTIVE 10mL
Active ingredientOCTINOXATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE
Label structure8 sections

Indications and uses

Indications and usage: After cleansing and toning regimen, apply a small amount onto face and neck area before exposing to outdoor sunlight, avoiding eye area. For optimal results, use after Ultimate Aqua Blanc Concentrate for an enhanced brightened complexion.

Dosage and administration

Dosage and administration: Take an adequate amount of this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Ethylhexyl Methoxycinnamate 7.5%, Ethylhexyl Salicylate 5%, Octocrylene 4%, Butyl Methoxydibenzoylmethane 3%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:
AQUA, BUTYLENE GLYCOL, METHYL METHACRYLATE CROSSPOLYMER, SILICA, CAPRYLIC/ CAPRIC TRIGLYCERIDE, NIACINAMIDE, GLYCERYL STEARATE, CETEARYL OLIVATE, CETEARYL ALCOHOL, SORBITAN OLIVATE, DIMETHICONE, PEG-100 STEARATE, POLY-SORBATE 60, NELUMBO NUCIFERA CALLUS CULTURE EXTRACT, XANTHAN GUM, PHENOXYETHANOL, TOCOPHERYL ACETATE, FRAGRANCE, SODIUM BENZOATE, POLYACRYLATE-13, SORBITAN STEARATE, DISODIUM EDTA, ROYAL JELLY EXTRACT, PEARL EXTRACT, GLYCERIN, POLYISOBUTENE, POTASSIUM SORBATE, CUCUMIS SATIVUS (CUCUMBER) FRUIT EXTRACT, NELUMBO NUCIFERA FLOWER EXTRACT, BHT, PROPYLENE GLYCOL, VACCINIUM MACROCARPON (CRANBERRY) FRUIT EXTRACT, OLEA EUROPAEA (OLIVE) LEAF EXTRACT, EQUISETUM ARVENSE EXTRACT, ADANSONIA DIGITATA SEED EXTRACT, SORBITAN ISOSTEARATE, POLYSORBATE 20, USNEA BARBATA (LICHEN) EXTRACT, ZANTHOXYLUM PIPERITUM FRUIT EXTRACT, PULSATILLA KOREANA EXTRACT, VERONICA OFFICINALIS EXTRACT, PRIMULA VERIS EXTRACT, MENTHA PIPERITA (PEPPERMINT) LEAF EXTRACT, MELISSA OFFICINALIS LEAF EXTRACT, MALVA SYLVESTRIS (MALLOW) EXTRACT, ALCHEMILLA VULGARIS EXTRACT, ACHILLEA MILLEFOLIUM EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, SOPHORA JAPONICA FLOWER EXTRACT, SODIUM HYALURONATE, FRUCTAN, CAPRYLYL GLYCOL, ACETYL TYROSINE, 1,2- HEXANEDIOL, PAEONIA SUFFRUTICOSA ROOT EXTRACT, PUERARIA LOBATA ROOT EXTRACT, ETHYLHEXYLGLYCERIN

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sun Protective Lotion

WARNINGS

WARNINGS SECTION

Warnings:
Store in a cool environment.
Avoid contact with eyes.
In case of contact with eyes, rinse thoroughly with water.
If you experience any discomfort or allergic reaction after use, cease use immediately and consult with a doctor or skincare professional.
For external use only.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Indications and usage:
After cleansing and toning regimen, apply a small amount onto face and neck area before exposing to outdoor sunlight, avoiding eye area.
For optimal results, use after Ultimate Aqua Blanc Concentrate for an enhanced brightened complexion.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage and administration: Take an adequate amount of this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69015-110-012019-11-27C16284748780-19855e2a2-3915-60a7-e053-dbdaa90a05bdae1212e8-8325-482a-b8a0-03fdc155e565

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69015-110-01ULTIMATE AQUA BLANC PROTECTIVE10mL10 mL in 1 CARTONLOTION101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69015-110ULTIMATE AQUA BLANC PROTECTIVE 10ML (OCTINOXATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE) LOTION [RACINNE (HONG KONG) LIMITED]1Legacy NDC, 1 package rows20140625_ae1212e8-8325-482a-b8a0-03fdc155e565.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX1
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
OCTOCRYLENEACTIVE INGREDIENT5A68WGF6WM1
AVOBENZONEACTIVE MOIETYG63QQF2NOX1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
OCTOCRYLENEACTIVE MOIETY5A68WGF6WM1
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RA1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69015-11069015-110-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML · Source PDF

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 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 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
b3bf2015-0b08-46a0-b3ab-87a80e952f12ae1212e8-8325-482a-b8a0-03fdc155e5652014-06-25WarningsExact identifier
spl id: b3bf2015-0b08-46a0-b3ab-87a80e952f12
spl set id: ae1212e8-8325-482a-b8a0-03fdc155e565

Reported adverse events (FAERS/openFDA)#

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