NDC 67225-0023 Age 20s Essence Cover Pact Original White Latte 23

Titanium Dioxide, Ethylhexyl Methoxycinnamate, Octocrylene

NDC Product Code 67225-0023

NDC CODE: 67225-0023

Proprietary Name: Age 20s Essence Cover Pact Original White Latte 23 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: Titanium Dioxide, Ethylhexyl Methoxycinnamate, Octocrylene 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

  • 67225 - Aekyung Industrial Co., Ltd.
    • 67225-0023 - Age 20s Essence Cover Pact Original White Latte 23

NDC 67225-0023-1

Package Description: 2 CASE in 1 PACKAGE > 12.5 g in 1 CASE

NDC Product Information

Age 20s Essence Cover Pact Original White Latte 23 with NDC 67225-0023 is a a human over the counter drug product labeled by Aekyung Industrial Co., Ltd.. The generic name of Age 20s Essence Cover Pact Original White Latte 23 is titanium dioxide, ethylhexyl methoxycinnamate, octocrylene. The product's dosage form is cream and is administered via topical form.

Labeler Name: Aekyung Industrial 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.

Age 20s Essence Cover Pact Original White Latte 23 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 1.1075 g/12.5g
  • OCTINOXATE .875 g/12.5g
  • OCTOCRYLENE .5 g/12.5g

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.

  • HYALURONIC ACID (UNII: S270N0TRQY)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
  • FERROSOFERRIC OXIDE (UNII: XM0M87F357)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
  • MICA (UNII: V8A1AW0880)
  • C30-45 OLEFIN (UNII: 6DWD51M0O8)
  • C30-45 ALKYL METHICONE (UNII: NFX970DSI2)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • NIACINAMIDE (UNII: 25X51I8RD4)
  • CANDELILLA WAX (UNII: WL0328HX19)
  • HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
  • MONOSODIUM GLUTAMATE (UNII: W81N5U6R6U)
  • CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
  • VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
  • P-ANISIC ACID (UNII: 4SB6Y7DMM3)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • DIPROPYLENE GLYCOL (UNII: E107L85C40)
  • CETEARYL NONANOATE (UNII: F6ZWV2F361)
  • ADENOSINE (UNII: K72T3FS567)
  • LAVANDULA ANGUSTIFOLIA WHOLE (UNII: 51217XIL5L)
  • ORIGANUM VULGARE SUBSP. HIRTUM WHOLE (UNII: 38SNL0F81Z)
  • POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
  • ROSMARINUS OFFICINALIS WHOLE (UNII: EA3289138M)
  • THYMUS VULGARIS WHOLE (UNII: 8L72OKJ7II)
  • WATER (UNII: 059QF0KO0R)
  • LEMON (UNII: 24RS0A988O)
  • CASEIN (UNII: 48268V50D5)
  • PEARL (HYRIOPSIS CUMINGII) (UNII: A75L5FZ40U)
  • KAKADU PLUM (UNII: 0ZQ1D2FDLI)
  • YEAST (UNII: 3NY3SM6B8U)
  • CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)
  • AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • MADECASSOSIDE (UNII: CQ2F5O6YIY)
  • DIAMOND (UNII: 6GRV67N0U2)
  • PENTYLENE GLYCOL (UNII: 50C1307PZG)
  • 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
  • SODIUM LACTATE (UNII: TU7HW0W0QT)
  • HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • ZINC OXIDE (UNII: SOI2LOH54Z)
  • PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
  • NEPIDERMIN (UNII: TZK30RF92W)
  • PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
  • DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
  • POMEGRANATE JUICE (UNII: 99S671U9KB)
  • SAUSSUREA INVOLUCRATA WHOLE (UNII: C7X2ALW7JZ)
  • ROYAL JELLY (UNII: L497I37F0C)
  • SOYBEAN GERM (UNII: JBW2VHD14M)

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: Aekyung Industrial Co., Ltd.
Labeler Code: 67225
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: 12-02-2019 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: 12-31-2020 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’.

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Age 20s Essence Cover Pact Original White Latte 23 Product Label Images