FDA.reportPublic FDA data

PROVENCE CALENDULA DAILY SUN BLOCK

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2015-05-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:31:55

Label at a glance#

ProductPROVENCE CALENDULA DAILY SUN BLOCK
Active ingredientOCTINOXATE, TITANIUM DIOXIDE, AVOBENZONE, OCTISALATE, OCTOCRYLENE
Label structure7 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: ETHYLHEXYL METHOXYCINNAMATE 7.50%, TITANIUM DIOXIDE (CI 77891) 5.95%, BUTYL METHOXYDIBENZOYLMETHANE 2.50%, ETHYLHEXYL SALICYLATE 2.00%, OCTOCRYLENE 2.00%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: WATER, CYCLOPENTASILOXANE, GLYCERIN,ETHYLHEXYL PALMITATE,CYCLOHEXASILOXANE,4-METHYLBENZYLIDENE CAMPHOR,NIACINAMIDE,NEOPENTYL GLYCOL DIHEPTANOATE,BUTYLENE GLYCOL, SILICA,CETEARYL ALCOHOL,GLYCERYL STEARATE,PEG-100 STEARATE,TRICETEARETH-4 PHOSPHATE,GLYCOL STEARATE,SORBITAN SESQUIOLEATE,POTASSIUM CETYL PHOSPHATE,PEG-2 STEARATE,ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER,FRAGRANCE(PARFUM),TROMETHAMINE,GLYCERYL CAPRYLATE,PHENOXYETHANOL,CAPRYLYL GLYCOL,DIMETHICONE,ADENOSINE,XANTHAN GUM,IRON OXIDES (CI 77492),DISODIUM EDTA,CALENDULA OFFICINALIS FLOWER EXTRACT,IRON OXIDES (CI 77491),ANTHEMIS NOBILIS FLOWER WATER,SODIUM BENZOATE,CITRIC ACID,POTASSIUM SORBATE

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen [UV Protection]

CAUTIONS

WARNINGS SECTION

CAUTIONS: 1. For external use only. 2. Discontinue use if signs of irritation or rashes appear. 3. Keep out of reach of children 4. 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

HOW TO USE

DESCRIPTION SECTION

HOW TO USE: Take an adequate amount of the product and thoroughly apply on the areas exposed to the UV rays.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138806173420407GTIN-13: 8806173420407
EAN-13: 8806173420407
GTIN storage (14 digits): 08806173420407		provence calendula daily sun block carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-284-012020-02-20C16284748780-19d75b9d0-1996-f424-e053-dadaa90a57ce023dfed8-9787-459d-90dd-1c6b0c6d6d18
51346-284-012020-01-31C16284748780-19d75b9d0-1996-f424-e053-dadaa90a57ce023dfed8-9787-459d-90dd-1c6b0c6d6d18

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
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
51346-28451346-284-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB
WATER059QF0KO0RIACT

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
be783590-147c-4f5b-a242-d88c33f08679023dfed8-9787-459d-90dd-1c6b0c6d6d182015-05-19WarningsExact identifier
spl id: be783590-147c-4f5b-a242-d88c33f08679
spl set id: 023dfed8-9787-459d-90dd-1c6b0c6d6d18

Reported adverse events (FAERS/openFDA)#

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