FDA.reportPublic FDA data

UV LOCK FLOWER WATER GEL SUN

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2013-05-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:40:43

Label at a glance#

ProductUV LOCK FLOWER WATER GEL SUN SPF30 PA PLUS PLUS
Active ingredientOCTINOXATE, OCTISALATE
Label structure8 sections

Indications and uses

How to Use: Evenly apply an appropriate amount to skin that can be easily exposed to UV rays.

Dosage and administration

How to Use: Evenly apply an appropriate amount to skin that can be easily exposed to UV rays.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: ETHYLHEXYL METHOXYCINNAMATE 6%, ETHYLHEXYL SALICYLATE 3%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
WATER, CYCLOPENTASILOXANE, BUTYLENE GLYCOL, ISOAMYL P-METHOXYCINNAMATE, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, NIACINAMIDE, TRIETHANOLAMINE, GLYCERIN, DIPROPYLENE GLYCOL, PEG/PPG-30/10 DIMETHICONE, CARBOMER, CAPRYLYL GLYCOL, BEHENYL ALCOHOL, CETETH-10, FRAGRANCE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ALOE BARBADENSIS LEAF JUICE, ANTHEMIS NOBILIS FLOWER EXTRACT, HAMAMELIS VIRGINIANA FLOWER WATER, NELUMBO NUCIFERA FLOWER WATER, CAPRYLHYDROXAMIC ACID, ADENOSINE, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Cautions:
For external use only.
Avoid contact with eyes and mouth.
Discontinue use if signs of irritation or rashes appear.
Keep out of reach of children.
Replace the cap after use.

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

How to Use: Evenly apply an appropriate amount to skin that can be easily exposed to UV rays.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use: Evenly apply an appropriate amount to skin that can be easily exposed to UV rays.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-214-012020-02-28C16284748780-19d75b9cf-e49b-f424-e053-dadaa90a57ce25368f13-398b-4e42-b685-3b0e799cfd66
51346-214-012020-01-31C16284748780-19d75b9cf-e49b-f424-e053-dadaa90a57ce25368f13-398b-4e42-b685-3b0e799cfd66

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
NIACINAMIDEINACTIVE INGREDIENT25X51I8RD41
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-21451346-214-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
WATER059QF0KO0RIACT
NIACINAMIDE25X51I8RD4IACT

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 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
NIACINAMIDENIACINAMIDE25X51I8RD4CREAM / TOPICALNAExact identifier — unii candidate
4 equally ranked IID candidates
NIACINAMIDENIACINAMIDE25X51I8RD4GEL / TOPICAL25 mgExact identifier — unii candidate
4 equally ranked IID candidates
NIACINAMIDENIACINAMIDE25X51I8RD4INJECTION / INTRAMUSCULAR2.5 %w/vExact identifier — unii candidate
4 equally ranked IID candidates
NIACINAMIDENIACINAMIDE25X51I8RD4INJECTION / INTRAVENOUS2.5 %w/vExact identifier — unii candidate
4 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
7edd72a4-deb5-4760-a745-f967d01dd9e625368f13-398b-4e42-b685-3b0e799cfd662020-02-27WarningsExact identifier
spl set id: 25368f13-398b-4e42-b685-3b0e799cfd66

Reported adverse events (FAERS/openFDA)#

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