FDA.reportPublic FDA data

SKIN 79 Super Plus Beblesh Balm SPF25 PA (40g)

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 22:23:02

Label at a glance#

ProductSKIN 79 Super Plus Beblesh Balm SPF25 PA (40g)
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure3 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABEL
LABEL




OTC - ACTIVE INGREDIENT SECTION

INGREDIENTS:

Water, Propylene Glycol, Cyclomethicone, Dimethicone, Titanium Dioxide, Isopropyl Palmitate, Talc, Ethylhexyl Methoxycinnamate, Butylene Glycol, Dicaprylate/Dicaprate, Prunus Amygdalus Delcis (Sweet Almond) Oil, Ethylhexyl Salicylate, Digenlacrythrityl Hexahydroxystearate/Hexastearate/Hexarosinate, Cetyl PEG/PPG-10/1 Dimethicone, Arbulia, Zinc Oxide, Polyglyceryl-4 Isostearate, Magnesium Sulfate, Dimethicone[Vinyl] Dimethicone Crosspolymer, Iron Oxides, Silica, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Portulaca Oleracea Extract, Piper Methyslicum Leaf/Root/Steam Extract, Phenoxyethanol, Trihydroxystearia, Disteardimonium Hectorite, Glycosyl Trichalose, Aluminum Hydroxide, Aluminum Stearate, Methylparaben, Hydrogenated Starch Hydrolysate, Methicone, Tocopheryl Acetate, Propylparaben, Fragrance, Hydrogenated Lecithin, Citrus Umshiu Fruit Oil, Cholesterol, Ceramide 3, Nelumbo Nucifera Flower Water, Medocassoside, Caviar Extract, Camellia Sipcasis Leaf Extract, Aloe Barbedensis Leaf Juice, Lycium Chinenese Fruit Extract, Hellanthus Annus (Sun Flower) Extract, Schizandra Chinensis Fruit Extract, Hedera Helix (Ivy) Extract, Cornus Officixalis Fruit Extract, Bubylparaben, Glycerin, Adenosine, Caprylic/capric Triglyceride, Triclosan, Phytic Acid, Ubiquinose, BHT, Gold

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
49715-002-012019-10-21C16284748780-1956f9ecf-c9b4-621f-e053-dbdaa90a74ad83034652-aaf9-4183-9296-8a38261dea42

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49715-002-01SKIN 79 Super Plus Beblesh Balm SPF25 PA (40g)40 g in 1 BOTTLE, PLASTICCREAM401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49715-002SKIN 79 SUPER PLUS BEBLESH BALM SPF25 PA (40G) (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [WIZCOZ CORPORATION LTD]1Legacy NDC, 1 package rows20091217_83034652-aaf9-4183-9296-8a38261dea42.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
49715-00249715-002-01

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
DIMETHICONE92RU3N3Y1OIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
ZINC OXIDESOI2LOH54ZACTIB

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 HYDROXIDE5QB0T2IUN0TABLET / ORAL50 mgExact identifier — unii candidate
4 equally ranked IID candidates
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 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
5373e6a1-1175-4dd8-ac66-e400f206f99883034652-aaf9-4183-9296-8a38261dea422009-11-09Exact identifier
spl id: 5373e6a1-1175-4dd8-ac66-e400f206f998
spl set id: 83034652-aaf9-4183-9296-8a38261dea42

Reported adverse events (FAERS/openFDA)#

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