FDA.reportPublic FDA data

SKIN 79 The Prestige Beblesh Balm (5g)

Manufacturer
WIZCOZ CORPORATION LTD
Effective date
2009-11-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:23:03

Label at a glance#

ProductSKIN 79 The Prestige Beblesh Balm (5g)
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure3 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BOX LABEL
BOX LABEL

OTC - ACTIVE INGREDIENT SECTION


INGREDIENTS:

WATER, TITANIUM DIOXIDE, CYCLOPENTASILOXANE, PHENYL TRIMETHICONE, BUTYLENE GLYCOL, BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE, ZINC OXIDE, DIMETHICONE, C12-15 ALKYL BENZOATE, CETYL PEG/PPG-10/1 DIMETHICONE, HYDROGENATED POLYDECENE, ARBUTIN, HEXYL LAURATE, POLYGLYCERYL-4 ISOSTEARATE, SORBITAN ISOSTEARATE, NATTO GUM, GLYCERIN, MICA, CYCLOHEXASILOXANE, TALC, SORBITAN OLIVATE, OZOKERITE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, SODIUM CHLORIDE, DISTEARDIMONIUM HECTORITE, ALUMINUM HYDROXIDE, STEARIC ACID, TRIEHOXYCAPRYLSILANE, DIMETHICONE/METHICONE COPOLYMER, CALCIUM STEARATE, PROPYLENE CARBONATE, TOCOPHEROL ACETATE, HUMAN OLIGOPEPTIDE-1, ALOE BARBADENSIS LEAF JUICE, HYDROLIZED COLLAGE, NELUMBIUM SPECIOSUM FLOWER EXTRACT, CAVIAR EXTRACT, UBIQUINONE, PORTULACA OLERACEA EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, ACETYL HEXAPEPTIDE-8, ADENOSINE, DISODIUM EDTA, ASPARAGUS LUCIDUS ROOT EXTRACT, TUSSILAGO FARFARA (COLTSFOOT) FLOWER EXTRACT, LAMINARIA JAPONICA EXTRACT, DIAMOND POWDER, AMETHYST POWDER, PEARL POWDER, CORAL POWDER, TOURMALIN, CERAMIDE 3, GOLD, HESPERIDIN METHYL CHALCONE, STEARETH-20, DIPEPTIDE-2, PALMITOYL TETRAPEPTIDE-7, COPPER TRIPEPTIDE-1, LECITHIN, DEA-CETYL PHOSPHATE, RETINYL PALMITATE, SUCROSE DISTEARATE, SODIUM ASCORBYL PHOSPHATE, PANTHENOL, SILK AMINO ACIDES, ASCORBIN ACID, METHYLPARABEN, BUTYLPARABEN, PROPYLPARABEN, FRAGRANCE, IRON OXIDE RED, IRON OXIDE YELLOW, IRON OXIDE BLACK

OTC - WHEN USING SECTION

DIRECTIONS:

Use it proper quantity on the area of your face like patting at the last step of skin care.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49715-004-012019-10-21C16284748780-1956f9ecf-cc90-621f-e053-dbdaa90a74ad5f0fbe86-ae3b-4790-b4ce-b9b8b975708f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49715-004-01SKIN 79 The Prestige Beblesh Balm (5g)5 g in 1 BOTTLE, PLASTICCREAM51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49715-004SKIN 79 THE PRESTIGE BEBLESH BALM (5G) (ZINC OXIDE, TITANIUM DIOXIDE) CREAM [WIZCOZ CORPORATION LTD]1Legacy NDC, 1 package rows20091218_5f0fbe86-ae3b-4790-b4ce-b9b8b975708f.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
TITANIUMACTIVE MOIETYD1JT611TNE1
ZINCACTIVE MOIETYJ41CSQ7QDS1
ALUMINUM HYDROXIDEINACTIVE INGREDIENT5QB0T2IUN01
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1O1

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
49715-00449715-004-01

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 OXIDESOI2LOH54ZACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
DIMETHICONE92RU3N3Y1OIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT

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
ALUMINUM HYDROXIDEALUMINUM HYDROXIDE5QB0T2IUN0CREAM / TOPICAL5 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
ALUMINUM HYDROXIDEALUMINUM HYDROXIDE5QB0T2IUN0CAPSULE / ORALNAExact identifier — unii candidate
4 equally ranked IID candidates
ALUMINUM HYDROXIDEALUMINUM HYDROXIDE5QB0T2IUN0TABLET / ORAL50 mgExact identifier — unii candidate
4 equally ranked IID candidates
ALUMINUM HYDROXIDEALUMINUM HYDROXIDE5QB0T2IUN0OINTMENT / TOPICALNAExact 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
9e62e349-eb9a-466b-9f27-f97e8f9555155f0fbe86-ae3b-4790-b4ce-b9b8b975708f2009-11-09Exact identifier
spl id: 9e62e349-eb9a-466b-9f27-f97e8f955515
spl set id: 5f0fbe86-ae3b-4790-b4ce-b9b8b975708f

Reported adverse events (FAERS/openFDA)#

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