UV LOCK FLOWER DAILY POWERFUL 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 01:40:45

Label at a glance#

ProductUV LOCK FLOWER DAILY POWERFUL SUN SPF50PLUS PA PLUS PLUS PLUS
Active ingredientOCTINOXATE, Titanium Dioxide, AVOBENZONE, OCTISALATE, Octocrylene
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 7.5%, Titanium Dioxide 4.25%, Butyl Methoxydibenzoylmethane 2.5%, Ethylhexyl Salicylate 2%, Octocrylene 2%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Water, Ethylhexyl Palmitate, Cyclopentasiloxane, 4-Methylbenzylidene Camphor, Butylene Glycol, Niacinamide, Neopentyl Glycol Diheptanoate, Dipropylene Glycol, Cetearyl Alcohol, Cyclohexasiloxane, Glyceryl Stearate, Polysorbate 60, PEG-100 Stearate, Hydrogenated Poly(C6-14 Olefin),
Triceteareth-4 Phosphate, Glycol Stearate, Silica, Methyl Methacrylate Crosspolymer, Potassium Cetyl Phosphate, Polymethylsilsesquioxane, PEG-2 Stearate, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Glyceryl Caprylate, Beeswax, Phenoxyethanol,
Fragrance(Parfum), Caprylyl Glycol, Dimethicone, Water, Xanthan Gum, Disodium EDTA, Glycine Soja (Soybean) Oil, Iron Oxides (CI 77491), Iron Oxides (CI 77492), Oenothera Biennis (Evening Primrose) Oil, Helianthus Annuus (Sunflower) Seed Oil, Rosa Damascena Flower Oil,
Rosa Gallica Flower Extract, 1,2-Hexanediol, Glycyrrhiza Glabra (Licorice) Root Extract, Rosa Canina Fruit Extract, Centella Asiatica Extract, Hordeum Vulgare Extract, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract

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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809367210976GTIN-13: 8809367210976
EAN-13: 8809367210976
GTIN storage (14 digits): 08809367210976
uv lock flower daily powerful sun carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-208-012020-02-26C16284748780-19d75b9d0-3c01-f424-e053-dadaa90a57ce1d56e012-c668-4f2b-9989-ce923512acdc
51346-208-012020-01-31C16284748780-19d75b9d0-3c01-f424-e053-dadaa90a57ce1d56e012-c668-4f2b-9989-ce923512acdc

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX1
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
OctocryleneACTIVE INGREDIENT5A68WGF6WM1
Titanium DioxideACTIVE INGREDIENT15FIX9V2JP1
AVOBENZONEACTIVE MOIETYG63QQF2NOX1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
OCTOCRYLENEACTIVE MOIETY5A68WGF6WM1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
Ethylhexyl PalmitateINACTIVE INGREDIENT28659933091
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-20851346-208-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
568e0f98-1f01-4aee-bcc7-7b27636cc8401d56e012-c668-4f2b-9989-ce923512acdc2013-05-29WarningsExact identifier
spl id: 568e0f98-1f01-4aee-bcc7-7b27636cc840
spl set id: 1d56e012-c668-4f2b-9989-ce923512acdc

Reported adverse events (FAERS/openFDA)#

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