FDA.reportPublic FDA data

Cellromax 7 Signature CC Cream

Manufacturer
PHARMACIST&HEALTH CO., LTD. | FINECOS
Effective date
2020-11-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:33:47

Label at a glance#

ProductCellromax 7 Signature CC Cream
Active ingredientTITANIUM DIOXIDE, OCTINOXATE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethylhexyl Methoxycinnamate 7.4%, Titanium Dioxide 6.3%

INACTIVE INGREDIENT SECTION

Water, Cyclopentasiloxane, Cyclohexasiloxane, Dimethicone, Glycerin, 4-Methylbenzylidene Camphor, Dipropylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Phenyl Trimethicone, Silica, Hydrogenated Polyisobutene, Sorbitan Isostearate, Methyl Gluceth-20, Polyglyceryl-2 Oleate, Sodium Chloride, Trihydroxystearin, Polyhydroxystearic Acid, Mica, CI 77492, Bentonite, PEG-10 Dimethicone, Dimethicone/Vinyl Dimethicone Crosspolymer, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Polymethyl Methacrylate, Polyglyceryl-2 Stearate, Chlorphenesin, Ethylhexylglycerin, Caprylyl Glycol, Methyl Trimethicone, Ceresin, CI 77491, CI 77499, Triethoxycaprylylsilane, Butylene Glycol, Tocopheryl Acetate, Tropolone, Ultramarines, 1,2-Hexanediol, Disodium EDTA, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Argania Spinosa Kernel Oil, Carthamus Tinctorius (Safflower) Seed Oil, Fragrance, Sodium Hyaluronate, Hydrolyzed Hyaluronic Acid, Hyaluronic Acid, Phenoxyethanol, Aloe Barbadensis Leaf Extract, Maltodextrin, Grifola Frondosa Fruiting Body Extract, Fomes Officinalis (Mushroom) Extract, Sucrose Dilaurate, Panthenol, Hydrolyzed Lupine Protein, Polysorbate 20, Escin, Pisum Sativum (Pea) Extract, Ruscus Aculeatus Root Extract, Ammonium Glycyrrhizate, Centella Asiatica Leaf Extract, Hydrolyzed Yeast Protein, Calendula Officinalis Flower Extract, p-Anisic Acid, PEG-40 Hydrogenated Castor Oil, Sodium Citrate, Sorbic Acid, rh-Polypeptide-3, rh-Polypeptide-64

DESCRIPTION SECTION

Directions: 1. Apply after basic skin care product. 2. Spread an appropriate amount over the entire face following the skin texture. 3. Reapply as required.

OTC - STOP USE SECTION

Do not use on damaged or broken Skin. Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children.

WARNINGS SECTION

For external use only.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cellromax seven signature cc creamCellromax seven signature cc cream

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79895-103-022022-01-28C16284748780-1d6a99b39-b378-a426-e053-dadaa90af4c2b444384e-3a1b-5526-e053-2a95a90a9ff7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79895-103-01Cellromax 7 Signature CC Cream50 mL in 1 CONTAINERCREAM501
79895-103-02Cellromax 7 Signature CC Cream1 in 1 BOXCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79895-103CELLROMAX 7 SIGNATURE CC CREAM (ETHYLHEXYL METHOXYCINNAMATE, TITANIUM DIOXIDE CREAM) CREAM [PHARMACIST&HEALTH CO., LTD.]1Legacy NDC, 2 package rows20201117_b444384e-3a1b-5526-e053-2a95a90a9ff7.zip

Products#

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

DailyMed product names page 1 of 2 · 68 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79895-10379895-103-01, 79895-103-02

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 66 matching rows.

Name, UNII, Kind table
NameUNIIKind
GELATIN HYDROLYSATE (PORCINE SKIN, MW 3000)0K9R94573CIACT
HYDROGENATED POLYBUTENE (1300 MW)7D1YQ9Y5EZIACT
CYCLOMETHICONE 6XHK3U310BAIACT
LARICIFOMES OFFICINALIS FRUITING BODY7IFM8431X3IACT
TRIHYDROXYSTEARIN06YD7896S3IACT
MAITAKEA1U5YJI0Z8IACT
POLYSORBATE 207T1F30V5YHIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
EDETATE DISODIUM7FLD91C86KIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
PANTHENOLWV9CM0O67ZIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
SORBIC ACIDX045WJ989BIACT
FERRIC OXIDE RED1K09F3G675IACT
ARGAN OIL4V59G5UW9XIACT
SODIUM CITRATE1Q73Q2JULRIACT
DIMETHICONE92RU3N3Y1OIACT
SODIUM CHLORIDE451W47IQ8XIACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)9E4CO0W6C5IACT
CHLORPHENESINI670DAL4SZIACT
SUCROSE DILAURATE5926LC4S7MIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
SAFFLOWER OIL65UEH262ISIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
PHENOXYETHANOLHIE492ZZ3TIACT
P-ANISIC ACID4SB6Y7DMM3IACT
AMMONIUM GLYCYRRHIZATE3VRD35U26CIACT
POLY(METHYL METHACRYLATE; 450000 MW)Z47NNT4J11IACT
CAPRYLYL GLYCOL00YIU5438UIACT
RUSCUS ACULEATUS ROOTZW12V95I1QIACT
ALMOND OIL66YXD4DKO9IACT
POLYGLYCERYL-2 STEARATE253MC0P0YVIACT
MICAV8A1AW0880IACT
TROPOLONE7L6DL16P1TIACT
METHYL TRIMETHICONES73ZQI0GXMIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CERESINQ1LS2UJO3AIACT
GLYCERINPDC6A3C0OXIACT
ENZACAMENE8I3XWY40L9IACT
DIPROPYLENE GLYCOLE107L85C40IACT

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
b444384e-3a1c-5526-e053-2a95a90a9ff7b444384e-3a1b-5526-e053-2a95a90a9ff72020-11-16WarningsExact identifier
spl id: b444384e-3a1c-5526-e053-2a95a90a9ff7
spl set id: b444384e-3a1b-5526-e053-2a95a90a9ff7

Reported adverse events (FAERS/openFDA)#

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