NDC 71909-0054 Lovluv Daily Bb Cream

Titanium Dioxide, Ethylhexyl Methoxycinnamate, Zinc Oxide, Ethylhexyl Salicylate

NDC Product Code 71909-0054

NDC Code: 71909-0054

Proprietary Name: Lovluv Daily Bb 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: Titanium Dioxide, Ethylhexyl Methoxycinnamate, Zinc Oxide, Ethylhexyl Salicylate 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

  • 71909 - Cnt Dream Co.,ltd
    • 71909-0054 - Lovluv Daily Bb Cream

NDC 71909-0054-1

Package Description: 500 POUCH in 1 BOX > 1 g in 1 POUCH (71909-0054-0)

NDC Product Information

Lovluv Daily Bb Cream with NDC 71909-0054 is a a human over the counter drug product labeled by Cnt Dream Co.,ltd. The generic name of Lovluv Daily Bb Cream is titanium dioxide, ethylhexyl methoxycinnamate, zinc oxide, ethylhexyl salicylate. The product's dosage form is cream and is administered via topical form.

Labeler Name: Cnt Dream 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.

Lovluv Daily Bb 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.

  • OCTINOXATE .75 g/15g
  • TITANIUM DIOXIDE 1.05 g/15g
  • ZINC OXIDE .6015 g/15g
  • OCTISALATE .15 g/15g

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)

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.

Product Labeler Information

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

Labeler Name: Cnt Dream Co.,ltd
Labeler Code: 71909
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: 02-20-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 02-19-2020 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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.

Lovluv Daily Bb 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 Section

Titanium Dioxide 7% sunscreen

Ethylhexyl Methoxycinnamate 5% sunscreen

Zinc Oxide 4% sunscreen

Ethylhexyl Salicylate 1% sunscreen

Inactive Ingredient Section

Water, Methylpropanediol, CI 77492, Caprylic/Capric Triglyceride, Cyclopentasiloxane, Cyclomethicone, Cyclohexasiloxane, Arbutin, 1,2-Hexanediol, Cetyl PEG/PPG-10/1 Dimethicone, CI 77491, Ozokerite, Sorbitan Sesquioleate, PEG-10 Dimethicone, Sodium Chloride, CI 77499, Dimethicone/Vinyl Dimethicone Crosspolymer, Triethoxycaprylylsilane, Methicone, PEG/PPG-19/19 Dimethicone, Centella Asiatica Extract, Chamomilla Recutita (Matricaria) Flower Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Camellia Sinensis Leaf Extract, Polygonum Cuspidatum Root Extract,

Rosmarinus Officinalis (Rosemary) Leaf Extract, Scutellaria Baicalensis Root Extract, Sodium Hyaluronate, Xylitylglucoside, Anhydroxylitol, Xylitol, Ceramide NP, Jasminum Officinale Flower Oil, Ethylhexylglycerin, Adenosine

Otc- Ask Doctor Section

Stop use and ask a doctor if rash or irritation develops and lasts.

Otc- Do Not Use Section

Do not use on damaged or broken skin

Otc - Keep Out Of Reach Of Children Section

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Warning Section

Warnings

*For external use only

*Do not use on damaged or broken skin

*When using this product keep out of eyes, Rinse with water to remove.

*Stop use and ask a doctor if rash or irritation develops and lasts.

*Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Otc - Purpose Section

BB Cream

Indications & Usage Section

*helps prevent sunburn

*if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

* Please review the disclaimer below.

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