NDC 73393-010 La Muse Return 2 Blessing Visual

Octinoxate, Zinc Oxide, Octisalate, Titanium Dioxide, Octocrylene

NDC Product Code 73393-010

NDC 73393-010-02

Package Description: 1 CONTAINER in 1 CARTON > 15 mL in 1 CONTAINER (73393-010-01)

NDC 73393-010-04

Package Description: 1 CONTAINER in 1 CARTON > 30 mL in 1 CONTAINER (73393-010-03)

NDC Product Information

La Muse Return 2 Blessing Visual with NDC 73393-010 is a a human over the counter drug product labeled by Skinisgood. The generic name of La Muse Return 2 Blessing Visual is octinoxate, zinc oxide, octisalate, titanium dioxide, octocrylene. The product's dosage form is cream and is administered via topical form.

Labeler Name: Skinisgood

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.

La Muse Return 2 Blessing Visual 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.

  • OCTINOXATE 7.5 g/100mL
  • ZINC OXIDE 7.27 g/100mL
  • OCTISALATE 5 g/100mL
  • TITANIUM DIOXIDE 2.51 g/100mL
  • OCTOCRYLENE 1 g/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.

  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)

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: Skinisgood
Labeler Code: 73393
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: 10-01-2019 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’.

* Please review the disclaimer below.

La Muse Return 2 Blessing Visual Product Label Images

La Muse Return 2 Blessing Visual 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

Active Ingredient

Active Ingredients: Ethylhexyl Methoxycinnamate 7.50%, Zinc Oxide 7.27%, Ethylhexyl Salicylate 5.00%, Titanium Dioxide 2.51%, Octocrylene 1.00%

Inactive Ingredient

Inactive ingredients:Water, Glycerin, Butylene Glycol, Caprylic/Capric Triglyceride, Hydrogenated Polydecene, Polysorbate 60, Niacinamide, Dimethicone, 1,2-Hexanediol, Cyclopentasiloxane, Polyglyceryl-3 Methylglucose Distearate, 4-Methylbenzylidene Camphor, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Saccharomyces Ferment Filtrate, Squalane, Argania Spinosa Kernel Oil, Lavandula Angustifolia (Lavender) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Monarda Didyma Leaf Extract, Mentha Piperita (Peppermint) Leaf Extract, Freesia Refracta Extract, Sodium Hyaluronate, Arctium Lappa Root Extract, Phellinus Linteus Extract, Dioscorea Japonica Root Extract, Piper Methysticum Leaf/Root/Stem Extract, Origanum Vulgare Leaf Extract, Chamaecyparis Obtusa Leaf Extract, Salix Alba (Willow) Bark Extract, Lactobacillus/Soybean Ferment Extract, Portulaca Oleracea Extract, Cinnamomum Cassia Bark Extract, Scutellaria Baicalensis Root Extract, Panthenol, Raffinose, Folic Acid, Ceramide NP, Cholesterol, Tromethamine, Palmitoyl Pentapeptide-4, Cyclohexasiloxane, Glyceryl Stearate, Cetearyl Olivate, Arachidyl Alcohol, Sodium Polyacrylate, Sorbitan Olivate, Stearic Acid, Aluminum Hydroxide, Behenyl Alcohol, Triethoxycaprylylsilane, Arachidyl Glucoside, Hydrogenated Lecithin, Butyrospermum Parkii (Shea) Butter, Fragrance, Ethylhexylglycerin, Disodium EDTA, Adenosine, Cetearyl Alcohol, Palmitic Acid, Betaine, Glycosyl Trehalose, Glucose, Hydrogenated Starch Hydrolysate, Glyceryl Acrylate/Acrylic Acid Copolymer, CI 77492, CI 77491, Dipropylene Glycol, Lauric Acid, PVM/MA Copolymer, CI 77499, Myristic Acid, Isononyl Isononanoate

Purpose

PURPOSE: Sunscreen

Warnings

Warnings:For external use onlyDiscontinue use if signs of irritation or rashes appear.

Description

Uses:■ Helps prevent sunburn■ Can be used as a make-up baseDirections:■ Use it in the first step of your basic make up routine

Questions

Questions:If you have any questions about the product, please contact us.ysj@skinisgood.com+82 10 8725 8683

* Please review the disclaimer below.