NDC 79895-101 Cellromax 7 Signature Cc Cream

Ethylhexyl Methoxycinnamate, Titanium Dioxide

NDC Product Code 79895-101

NDC CODE: 79895-101

Proprietary Name: Cellromax 7 Signature Cc Cream What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Ethylhexyl Methoxycinnamate, Titanium Dioxide What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 79895 - Pharmacist&health Co., Ltd.

NDC 79895-101-02

Package Description: 1 CONTAINER in 1 BOX > 50 mL in 1 CONTAINER (79895-101-01)

NDC Product Information

Cellromax 7 Signature Cc Cream with NDC 79895-101 is a a human over the counter drug product labeled by Pharmacist&health Co., Ltd.. The generic name of Cellromax 7 Signature Cc Cream is ethylhexyl methoxycinnamate, titanium dioxide. The product's dosage form is cream and is administered via topical form.

Labeler Name: Pharmacist&health Co., Ltd.

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Cellromax 7 Signature Cc Cream Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • TITANIUM DIOXIDE 6.3 mg/100mL
  • OCTINOXATE 7.4 mg/100mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • PANTHENOL (UNII: WV9CM0O67Z)
  • CENTELLA ASIATICA LEAF (UNII: 6810070TYD)
  • SORBIC ACID (UNII: X045WJ989B)
  • BENTONITE (UNII: A3N5ZCN45C)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • ULTRAMARINE VIOLET (UNII: 1YZ11D167R)
  • ARGAN OIL (UNII: 4V59G5UW9X)
  • SODIUM CITRATE (UNII: 1Q73Q2JULR)
  • FIBROBLAST GROWTH FACTOR 7 (UNII: 9YXF283GP1)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
  • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
  • POLYGLYCERYL-2 STEARATE (UNII: 253MC0P0YV)
  • CHLORPHENESIN (UNII: I670DAL4SZ)
  • MICA (UNII: V8A1AW0880)
  • FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
  • TROPOLONE (UNII: 7L6DL16P1T)
  • METHYL TRIMETHICONE (UNII: S73ZQI0GXM)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • CERESIN (UNII: Q1LS2UJO3A)
  • GELATIN HYDROLYSATE (PORCINE SKIN, MW 3000) (UNII: 0K9R94573C)
  • PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
  • HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
  • FERROSOFERRIC OXIDE (UNII: XM0M87F357)
  • ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • POLYGLYCERYL-2 OLEATE (UNII: 5759J47SAM)
  • VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
  • ESCIN (UNII: RUU8G67GQM)
  • SUCROSE DILAURATE (UNII: 5926LC4S7M)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
  • SAFFLOWER OIL (UNII: 65UEH262IS)
  • LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
  • MALTODEXTRIN (UNII: 7CVR7L4A2D)
  • PEA (UNII: W4X7H8GYFM)
  • TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
  • 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ENZACAMENE (UNII: 8I3XWY40L9)
  • DIPROPYLENE GLYCOL (UNII: E107L85C40)
  • SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
  • METHYL GLUCETH-20 (UNII: J3QD0LD11P)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • MAITAKE (UNII: A1U5YJI0Z8)
  • HYALURONIC ACID (UNII: S270N0TRQY)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • P-ANISIC ACID (UNII: 4SB6Y7DMM3)
  • AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
  • CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
  • POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
  • AQUAPORIN-1 (UNII: 36141CLK2Y)
  • POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • RUSCUS ACULEATUS ROOT (UNII: ZW12V95I1Q)
  • ALMOND OIL (UNII: 66YXD4DKO9)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Pharmacist&health Co., Ltd.
Labeler Code: 79895
FDA Application Number: part352 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 10-27-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Cellromax 7 Signature Cc Cream Product Label Images

Cellromax 7 Signature Cc Cream Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Ethylhexyl Methoxycinnamate 7.4%, Titanium Dioxide 6.3%

Inactive Ingredient

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

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

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

Otc - Keep Out Of Reach Of Children

Keep Out of Reach of Children.

Warnings

For external use only.

* Please review the disclaimer below.