NDC 71261-011 Jungsaemmool Essential Skin Nuder Longwear Cushion Fair Light

Titanium Dioxide, Octinoxate, Zinc Oxide, Octisalate

NDC Product Code 71261-011

NDC CODE: 71261-011

Proprietary Name: Jungsaemmool Essential Skin Nuder Longwear Cushion Fair Light 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, Octinoxate, Zinc Oxide, Octisalate 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.

NDC Code Structure

  • 71261 - Jungsaemmool Beauty Co., Ltd.
    • 71261-011 - Jungsaemmool Essential Skin Nuder Longwear Cushion Fair Light

NDC 71261-011-02

Package Description: 2 CONTAINER in 1 CARTON > 14 g in 1 CONTAINER (71261-011-01)

NDC Product Information

Jungsaemmool Essential Skin Nuder Longwear Cushion Fair Light with NDC 71261-011 is a a human over the counter drug product labeled by Jungsaemmool Beauty Co., Ltd.. The generic name of Jungsaemmool Essential Skin Nuder Longwear Cushion Fair Light is titanium dioxide, octinoxate, zinc oxide, octisalate. The product's dosage form is cream and is administered via topical form.

Labeler Name: Jungsaemmool Beauty 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.

Jungsaemmool Essential Skin Nuder Longwear Cushion Fair Light 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 96 mg/g
  • OCTINOXATE 70 mg/g
  • ZINC OXIDE 49 mg/g
  • OCTISALATE 45 mg/g

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.

  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • CAMELLIA SINENSIS SEED OIL (UNII: O5R6DK2M9K)
  • SAFFLOWER OIL (UNII: 65UEH262IS)
  • CERAMIDE NP (UNII: 4370DF050B)
  • WATER (UNII: 059QF0KO0R)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • METHYL TRIMETHICONE (UNII: S73ZQI0GXM)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • NIACINAMIDE (UNII: 25X51I8RD4)
  • PENTYLENE GLYCOL (UNII: 50C1307PZG)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • PEG/PPG-17/6 COPOLYMER (UNII: P5QZM4T259)
  • MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
  • SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
  • FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
  • DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • FERROSOFERRIC OXIDE (UNII: XM0M87F357)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • ADENOSINE (UNII: K72T3FS567)
  • JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432)
  • NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
  • IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC)
  • LEONTOPODIUM NIVALE SUBSP. ALPINUM FLOWERING TOP (UNII: QQC1AK06RK)
  • LILIUM CANDIDUM BULB (UNII: AHG15J8AM0)
  • NARCISSUS PSEUDONARCISSUS FLOWER (UNII: L879RBF1WN)
  • SUNFLOWER OIL (UNII: 3W1JG795YI)
  • PANTHENOL (UNII: WV9CM0O67Z)

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: Jungsaemmool Beauty Co., Ltd.
Labeler Code: 71261
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: 07-16-2020 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.

Jungsaemmool Essential Skin Nuder Longwear Cushion Fair Light Product Label Images

Jungsaemmool Essential Skin Nuder Longwear Cushion Fair Light 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

Titanium Dioxide 9.6%


Octinoxate 7.0%


Zinc Oxide 4.9%


Octisalate 4.5%

Otc - Purpose

Sunscreen

Indications & Usage

Helps prevent sunburn

Dosage & Administration

Apply liberally 15 minutes before sun exposure. Reapply at least every two hoursSun protection measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 of higher and other sun protection measures including: 1) Limited time in the sun, especially from 10 am to 2 pm. 2) Wear long-sleeve shirts, pants, hats, and sunglassesAsk a doctor to use for children under 6 months

Warnings

For external use onlyDo not use on damaged or broken skinWhen using this product, keep out of eyes. Rinse with water to remove.Stop using and ask a doctor if rash occurs.

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

Inactive Ingredient

Water, Cyclopentasiloxane, Methyl Methacrylate Crosspolymer, Butylene Glycol, Methyl Trimethicone, Dimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Glycerin, Niacinamide, Pentylene Glycol, Silica, Caprylyl Methicone, Butylene Glycol Dicaprylate/Dicaprate, Lauryl PEG-10 Tris(Trimethylsiloxy)silylethyl Dimethicone, PEG/PPG-17/6 Copolymer, Magnesium Sulfate, Phenoxyethanol, Dimethicone/Vinyl Dimethicone Crosspolymer, Sorbitan Isostearate, Aluminum Hydroxide, Iron Oxides (CI 77492), Disteardimonium Hectorite, Stearic Acid, Triethoxycaprylylsilane, Iron Oxides (CI 77491), Fragrance(Parfum), Iron Oxides (CI 77499), Ethylhexylglycerin, Adenosine, Disodium EDTA, Camellia Sinensis Seed Oil, Carthamus Tinctorius (Safflower) Seed Oil, Ceramide NP, Helianthus Annuus (Sunflower) Seed Oil, Panthenol, Jasminum Officinale (Jasmine) Flower/Leaf Extract, Nelumbo Nucifera Flower Extract, Freesia Refracta Extract, Iris Ensata Extract, Iris Versicolor Extract, Leontopodium Alpinum Flower/Leaf Extract, Lilium Candidum Bulb Extract, Narcissus Pseudonarcissus (Daffodil) Flower Extract, Rose Extract

Other Safety Information

Protect the product in the container from excessive heat and direct sun

* Please review the disclaimer below.