NDC 11489-143 No7 Lift And Luminate Triple Action Day Cream Spf 30

Avobenzone,octisalate, Octocrylene

NDC Product Code 11489-143

NDC Code: 11489-143

Proprietary Name: No7 Lift And Luminate Triple Action Day Cream Spf 30 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: Avobenzone,octisalate, 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.


Code Structure
  • 11489 - Bcm Ltd
    • 11489-143 - No7 Lift And Luminate Triple Action Day Cream Spf 30

NDC 11489-143-01

Package Description: 1 TUBE in 1 CARTON > 25 g in 1 TUBE

NDC Product Information

No7 Lift And Luminate Triple Action Day Cream Spf 30 with NDC 11489-143 is a a human over the counter drug product labeled by Bcm Ltd. The generic name of No7 Lift And Luminate Triple Action Day Cream Spf 30 is avobenzone,octisalate, octocrylene. The product's dosage form is cream and is administered via topical form.

Labeler Name: Bcm 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.


No7 Lift And Luminate Triple Action Day Cream Spf 30 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.

  • AVOBENZONE .75 g/25g
  • OCTOCRYLENE 1.875 g/25g
  • OCTISALATE 1.25 g/25g

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)
  • ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • MICA (UNII: V8A1AW0880)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
  • TRIBEHENIN (UNII: 8OC9U7TQZ0)
  • PENTYLENE GLYCOL (UNII: 50C1307PZG)
  • AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • SHEA BUTTER (UNII: K49155WL9Y)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • DIMETHICONOL (40 CST) (UNII: 343C7U75XW)
  • ETHYLPARABEN (UNII: 14255EXE39)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
  • PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576)
  • VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
  • ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • DIPROPYLENE GLYCOL (UNII: E107L85C40)
  • DIMETHYLMETHOXY CHROMANOL (UNII: XBH432G01F)
  • POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • MORUS ALBA LEAF (UNII: M8YIA49Q2P)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
  • PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
  • POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • ALCOHOL (UNII: 3K9958V90M)
  • SILICON (UNII: Z4152N8IUI)
  • SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
  • HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
  • CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
  • ACETYL TYROSYLARGININE CETYL ESTER (UNII: 3M7W78X5IR)
  • ABELMOSCHUS MOSCHATUS WHOLE (UNII: M7QAW6696G)
  • ASIAN GINSENG (UNII: CUQ3A77YXI)

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: Bcm Ltd
Labeler Code: 11489
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: 01-17-2019 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.

No7 Lift And Luminate Triple Action Day Cream Spf 30 Product Label Images

No7 Lift And Luminate Triple Action Day Cream Spf 30 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

Carton Active Ingredients Section

Active ingredientsAvobenzone 3%Octisalate 5%Octocrylene 7.5%

Uses

Uses - helps prevent sunburn

Warnings

For external use onlyDo not use on damaged or broken skinWhen using this product keep out of eyes. Rinse with water to remove.

Ask A Doctor

Stop use and ask a doctor if rash occurs

Keep Out Of Reach Of Children

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

Directions

Directionsapply liberally 15 minutes before sun exposure.reapply at least every 2 hours.use a water resistant sunscreen if swimming or sweating.children under 6 months of age: Ask a doctor.Sun 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 value of 15 or higher and other sun protection measures including:Limit time in the sun, especially from 10 a.m - 2 p.m.wear long-sleeved shirts, pants, hats and sunglasses

Storage

Other informationprotect the product in this container from excessive heat and direct sunavoid contact with fabrics

Inactive Ingredients

Aqua (Water), C12-15 alkyl benzoate, Glycerin, Tribehenin, Alcohol denat., Butylene glycol, Aluminum starch octenylsuccinate, Dimethicone, Mica, Cetearyl alcohol, Butyrospermum parkii (Shea) butter, Cetearyl glucoside, Ammonium acryloyldimethyltaurate/VP copolymer, Phenoxyethanol, Potassium cetyl phosphate, Methylparaben, Dimethiconol, Ascorbyl glucoside, Parfum (Fragrance), Propylene glycol, Xanthan gum, Ethylparaben, Pentylene glycol, Sodium hyaluronate, Tocopheryl acetate, Hibiscus abelmoschus extract, Retinyl palmitate, Simethicone, Phyllanthus emblica fruit extract, Hydrolyzed rice protein, Tetrasodium EDTA, Sorbitan laurate, T-butyl alcohol, Potassium hydroxide, Carbomer, Panax ginseng root extract, Dipropylene glycol, Dimethylmoethoxy chromanol, Polysorbate 20, Hydroxyethylcellulose, Acetyl dipeptide-1 cetyl ester, Morus alba leaf extract, Sodium benzoate, Tocopherol, Palmitoyl tripeptide-1, Palmitoyl tetrapeptide-7, CI77891 (Titanium dioxide).

Description

No7 Lift & Luminare Triple Action Collection2 x 25 ml e 2 x 0.84 US Fl. Oz.The complete anti-aging skincare regime to target the three signs of aging: wrinkles look reduced, skin appears lifted and noticeably firmer and skin tone is more even. See younger looking skin in just 2 weeks.

Carton

Carton

* Please review the disclaimer below.

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