FDA.reportPublic FDA data

THE FLOWER UV INTENSE PACT

Manufacturer
THEFACESHOP CO., LTD.
Effective date
2010-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:13

Label at a glance#

ProductTHE FLOWER UV INTENSE PACT SPF50 PA NB21
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure4 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: TITANIUM DIOXIDE, ZINC OXIDE

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

MICA(CI 77019), TALC, METHYL METHACRYLATE CROSSPOLYMER, ETHYLHEXYL METHOXYCINNAMATE, BORON NITRIDE, PHENYL TRIMETHICONE, DIMETHICONE, SILICA,
ETHYLHEXYL PALMITATE, IRON OXIDES(CI 77492), TRIETHOXYCAPRYLYLSILANE, METHICONE, CAPRYLIC / CAPRIC TRIGLYCERIDE, METHYLPARABEN, FRAGRANCE, IRON OXIDES(CI 77491), HYDROGENATED LECITHIN, BUTYLPARABEN, IRON OXIDES(CI 77499), ROSA CANINA FLOWER, JASMINUM OFFICINALE (JASMINE) FLOWER, ANTHEMIS NOBILIS FLOWER POWDER, PHALAENOPSIS AMABILIS EXTRACT, DENDROBIUM PHALAENOPSIS FLOWER EXTRACT, CAMELLIA JAPONICA FLOWER EXTRACT, LILIUM CANDIDUM BULB EXTRACT, IMPATIENS BALSAMINA FLOWER EXTRACT, PELARGONIUM GRAVEOLENS EXTRACT, CALENDULA OFFICINALIS FLOWER EXTRACT, HIBISCUS ROSA-SINENSIS FLOWER/LEAF EXTRACT, TROPAEOLUM MAJUS FLOWER/LEAF/STEM EXTRACT

DESCRIPTION SECTION

Warnings:
When using this product
Keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if
Rash or irritation develops and lasts.

Directions:
Apply evenly before sun exposure and as needed.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51523-023-012019-10-21C16284748780-1956f9ecf-deab-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-023-01THE FLOWER UV INTENSE PACTSPF50 PA NB2112 g in 1 CARTONPOWDER121

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-023THE FLOWER UV INTENSE PACT SPF50 PA NB21 (ZINC OXIDE) POWDER [THEFACESHOP CO., LTD.]1Legacy NDC, 1 package rows20100715_1c89a96f-9013-49c8-8f79-d53d822ed24c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
TITANIUMACTIVE MOIETYD1JT611TNE1
ZINC CATIONACTIVE MOIETY13S1S8SF371

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51523-02351523-023-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB

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
60b44338-edd9-4ea6-b125-17940fd7e1401c89a96f-9013-49c8-8f79-d53d822ed24c2010-07-14Exact identifier
spl id: 60b44338-edd9-4ea6-b125-17940fd7e140
spl set id: 1c89a96f-9013-49c8-8f79-d53d822ed24c

Reported adverse events (FAERS/openFDA)#

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