NDC 72284-0001 Im Tone Up Multi Base

Octyl Methoxycinnamate, Homosalate, Octyl Salicylate, Titanium Dioxide

NDC Product Code 72284-0001

NDC Code: 72284-0001

Proprietary Name: Im Tone Up Multi Base Additional informationCallout TooltipWhat 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: Octyl Methoxycinnamate, Homosalate, Octyl Salicylate, Titanium Dioxide Additional informationCallout TooltipWhat 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.


Code Structure
  • 72284 - Normalest Co., Ltd.
    • 72284-0001 - Im Tone Up Multi Base

NDC 72284-0001-1

Package Description: 1 TUBE in 1 BOX > 50 mL in 1 TUBE

NDC Product Information

Im Tone Up Multi Base with NDC 72284-0001 is a a human over the counter drug product labeled by Normalest Co., Ltd.. The generic name of Im Tone Up Multi Base is octyl methoxycinnamate, homosalate, octyl salicylate, titanium dioxide. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Normalest Co., Ltd.

Dosage Form: Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2

Product Type: Human Otc Drug Additional informationCallout TooltipWhat 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.


Im Tone Up Multi Base Active Ingredient(s)

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

  • OCTINOXATE 3.5 g/50mL
  • HOMOSALATE 3 g/50mL
  • OCTISALATE 2.25 g/50mL
  • TITANIUM DIOXIDE 1.78 g/50mL

Inactive Ingredient(s)

Additional informationCallout TooltipAbout 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.

  • SQUALANE (UNII: GW89575KF9)
  • FOSFRUCTOSE (UNII: M7522JYX1H)
  • INVERT SUGAR (UNII: ED959S6ACY)
  • PULLULAN (UNII: 8ZQ0AYU1TT)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
  • OCTYLDODECANOL (UNII: 461N1O614Y)
  • FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • STANNIC OXIDE (UNII: KM7N50LOS6)
  • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
  • MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
  • MENTHA PIPERITA LEAF (UNII: A389O33LX6)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • WATER (UNII: 059QF0KO0R)
  • DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • POLYSORBATE 60 (UNII: CAL22UVI4M)
  • SALVIA HISPANICA SEED (UNII: NU0OLX06F8)
  • CENTELLA ASIATICA (UNII: 7M867G6T1U)
  • HOUTTUYNIA CORDATA WHOLE (UNII: O3E12ZLW5T)
  • PENTYLENE GLYCOL (UNII: 50C1307PZG)
  • HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
  • METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: 657L0NC5MT)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
  • AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
  • 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • EDETIC ACID (UNII: 9G34HU7RV0)
  • ECHIUM PLANTAGINEUM SEED OIL (UNII: PIB7XBU8XW)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • ALCOHOL (UNII: 3K9958V90M)
  • CARDIOSPERMUM HALICACABUM WHOLE (UNII: 185RQ97K0V)
  • MALVA SYLVESTRIS WHOLE (UNII: I01732476C)
  • PRIMULA VERIS (UNII: W6LFQ57E4M)
  • VERONICA OFFICINALIS WHOLE (UNII: 9EHR580PSP)
  • ALUMINUM STEARATE (UNII: U6XF9NP8HM)

Administration Route(s)

Additional informationCallout TooltipWhat 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.

Product Labeler Information

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Normalest Co., Ltd.
Labeler Code: 72284
FDA Application Number: part352 Additional informationCallout TooltipWhat 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. Additional informationCallout TooltipWhat 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: 03-06-2019 Additional informationCallout TooltipWhat 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 Additional informationCallout TooltipWhat 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 Additional informationCallout TooltipWhat 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.

Im Tone Up Multi Base Product Label Images

Im Tone Up Multi Base 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

Active ingredientsOctyl Methoxycinnamate 7%Homosalate 6%Octyl Salicylate 4.5%Titanium Dioxide 3.5%

Inactive Ingredient

Inactive ingredientsWater, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Dicaprylyl Carbonate, Propanediol, C12-15 Alkyl Benzoate, Cyclopentasiloxane, Glyceryl Stearate, PEG-100 Stearate, Polysorbate 60, Salvia Hispanica Seed Extract, Centella Asiatica Extract, Ammonium Acryloyldimethyltaurate/VP Copolymer, Houttuynia Cordata Extract, Pentylene Glycol, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Synthetic Fluorphlogopite, Methyl Methacrylate Crosspolymer, Phenoxyethanol, Squalane, Aluminum Stearate, Fragrance, Fructooligosaccharides, Polyhydroxystearic Acid, Saccharide, Hydrolysate, Pullulan, Alumina, 1,2-Hexanediol, Aluminum Hydroxide, Ethylhexylglycerin, Xanthan Gum, Octyldodecanol, Iron Oxides (CI 77492), Triethoxycaprylylsilane, Disodium EDTA, Sorbitan Isostearate, Iron Oxides (CI 77491), Echium Plantagineum Seed Oil, Butylene Glycol, Glycerin, Tin Oxide, Alcohol, Cardiospermum Halicacabum Flower/Leaf/Vine Extract, Helianthus Annuus (Sunflower) Seed Oil Unsaponifiables, Achillea Millefolium Extract, Alchemilla Vulgaris Extract, Malva Sylvestris (Mallow) Extract ,Melissa Officinalis Leaf Extract, Mentha Piperita (Peppermint) Leaf Extract, Primula Veris Extract, Veronica Officinalis Extract, Tocopherol, Sodium Hydroxide

* Please review the disclaimer below.

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