FDA.reportPublic FDA data

UV LOCK FLOWER NON CHEMICAL SUN

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2013-05-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:40:46

Label at a glance#

ProductUV LOCK FLOWER NON CHEMICAL SUN SPF50PLUS PA PLUS PLUS PLUS
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure8 sections

Indications and uses

How to Use: Gently shake the bottle 3-5 times before use, and evenly apply an appropriate amount to skin that can be easily exposed to UV rays.

Dosage and administration

How to Use: Gently shake the bottle 3-5 times before use, and 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: ZINC OXIDE 12.48%, TITANIUM DIOXIDE 2%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
CYCLOPENTASILOXANE, WATER, BUTYLENE GLYCOL, DICAPRYLYL CARBONATE, NIACINAMIDE, METHYL METHACRYLATE CROSSPOLYMER, PEG-10 DIMETHICONE, PORTULACA OLERACEA EXTRACT, DIMETHICONE, MAGNESIUM SULFATE, METHICONE, BIOSACCHARIDE GUM-1, POLYMETHYL METHACRYLATE, SILICA, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, PHENOXYETHANOL, ALUMINUM HYDROXIDE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, CALCIUM ALUMINUM BOROSILICATE, CAPRYLYL GLYCOL, FRAGRANCE, STEARIC ACID, ALOE BARBADENSIS LEAF JUICE, ANTHEMIS NOBILIS FLOWER EXTRACT, GLYCERYL CAPRYLATE, HAMAMELIS VIRGINIANA FLOWER WATER, NELUMBO NUCIFERA FLOWER WATER, POLYGLYCERYL-6 POLYRICINOLEATE, TOCOPHERYL ACETATE, MICROCRYSTALLINE CELLULOSE, ADENOSINE, CELLULOSE GUM, 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: Gently shake the bottle 3-5 times before use, and evenly apply an appropriate amount to skin that can be easily exposed to UV rays.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use: Gently shake the bottle 3-5 times before use, and 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
51346-212-012020-02-27C16284748780-19d75b9d1-17fa-f424-e053-dadaa90a57ced0757514-7472-4794-a9cb-435d01a2e17e
51346-212-012020-01-31C16284748780-19d75b9d1-17fa-f424-e053-dadaa90a57ced0757514-7472-4794-a9cb-435d01a2e17e

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC CATIONACTIVE MOIETY13S1S8SF371
DICAPRYLYL CARBONATEINACTIVE INGREDIENT609A3V1SUA1
WATERINACTIVE INGREDIENT059QF0KO0R1

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
51346-21251346-212-01

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
ZINC OXIDESOI2LOH54ZACTIM
TITANIUM DIOXIDE15FIX9V2JPACTIB
WATER059QF0KO0RIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT

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
8c84b705-8735-4c7d-bedd-c66dba9d5a19d0757514-7472-4794-a9cb-435d01a2e17e2013-05-29WarningsExact identifier
spl id: 8c84b705-8735-4c7d-bedd-c66dba9d5a19
spl set id: d0757514-7472-4794-a9cb-435d01a2e17e

Reported adverse events (FAERS/openFDA)#

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