Urban Legend Antioxidant Day Cream With Green Tea And Vitamin C Sunscreen Broad Spectrum Spf 30
Avobenzone, Octinoxate, Octisalate, Octocrylene
Bcm Ltd
Human Otc Drug
NDC 11489-154Urban Legend Antioxidant Day Cream With Green Tea And Vitamin C Sunscreen Broad Spectrum Spf 30 also known as Avobenzone, Octinoxate, Octisalate, Octocrylene is a human otc drug labeled by 'Bcm Ltd'. National Drug Code (NDC) number for Urban Legend Antioxidant Day Cream With Green Tea And Vitamin C Sunscreen Broad Spectrum Spf 30 is 11489-154. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in Urban Legend Antioxidant Day Cream With Green Tea And Vitamin C Sunscreen Broad Spectrum Spf 30 drug includes Avobenzone - 2.25 g/75g Octinoxate - .375 g/75g Octisalate - 3.75 g/75g Octocrylene - 5.625 g/75g . The currest status of Urban Legend Antioxidant Day Cream With Green Tea And Vitamin C Sunscreen Broad Spectrum Spf 30 drug is Active.
Drug Information:
| Drug NDC: | 11489-154 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Urban Legend Antioxidant Day Cream With Green Tea And Vitamin C Sunscreen Broad Spectrum Spf 30 |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate, Octocrylene |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Bcm Ltd |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Cream |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | AVOBENZONE - 2.25 g/75g
OCTINOXATE - .375 g/75g
OCTISALATE - 3.75 g/75g
OCTOCRYLENE - 5.625 g/75g
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. |
| Marketing Start Date: | 01 Jan, 2020 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 19 Jun, 2026 |
| 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. |
| Application Number: | part352 |
| 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. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | BCM Ltd
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | G63QQF2NOX
4Y5P7MUD51
4X49Y0596W
5A68WGF6WM
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 11489-154-01 | 1 TUBE in 1 CARTON (11489-154-01) / 75 g in 1 TUBE | 01 Jan, 2020 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Purpose sunscreen uses uses helps prevent sunburn
Product Elements:
Urban legend antioxidant day cream with green tea and vitamin c sunscreen broad spectrum spf 30 avobenzone, octinoxate, octisalate, octocrylene avobenzone avobenzone octinoxate octinoxate octisalate octisalate octocrylene octocrylene water alkyl (c12-15) benzoate glycerin tribehenin alcohol dimethicone aluminum starch octenylsuccinate cetearyl glucoside ammonium acryloyldimethyltaurate/vp copolymer potassium cetyl phosphate phenoxyethanol panthenol .alpha.-tocopherol acetate polysorbate 20 dimethiconol (2000 cst) caprylyl glycol ascorbyl glucoside xanthan gum sodium benzoate .alpha.-bisabolol, (+)- ethylhexylglycerin citric acid monohydrate sphinganine edetate sodium tetrahydrate dipropylene glycol potassium hydroxide tert-butyl alcohol dimethylmethoxy chromanol silica dimethyl silylate green tea leaf butylated hydroxytoluene
Indications and Usage:
Directions apply 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.
Warnings and Cautions:
Warnings for external use o nly do not use on damaged or broken skin when using this product keep out of eyes. rinse with water to remove.
Description:
Description sun protection and pore-fectly bright skin. it has to be an... this lightweight, non-clogging formula means it's suitable for daily use. plus, it contains powerful antioxidants, leaving skin glory-ously glowy! enhance the natural radiance of your skin. helps protect your complexion from the sun. double defence non-clogging sunscreen broad spectrum spf 30 dermatologically tested. 87% of women agreed their skin looked brighter/more radiant after 4 weeks of use.* *from user trials conducted on 115 women manufactured for the boots company plc nottingham england ng2 3aa. boots retail ireland dublin 12 ireland. dist. in the usa by boots retail usa, new york, ny 10005 made in the uk soapandglory.com
Tube wording soap & glory urban legend antioxidant day cream with green tea and vitamin c sunscreen broad spectrum spf 30 this lightweight, non-clogging formula means it's suitable for daily use. plus, it contains powerful antioxidants, leaving skin glory-ously glowy! enhance the natural radiance of your skin, wh ile h elping protect to your complexion from the sun with our double-defence, non-clogging, protecting day cream. every day, apply liberally cheeks, chin & forehead. using our fingertips, gently blend into the skin making sure every last little bit is covered. warning: avoid contact with the eyes. if contact with eyes occurs, rinse thoroughly with warm water. this product is not designed for sunbathing. avoid contact with fabric. active ingredients: avobenzone 3% octinoxate 0.5% octisalate 5% octocrylene 7.5% manufactured for the boots company plc nottingham england ng2 3aa. boots retail ireland dublin 12 ireland. dist. in the usa by boots retail usa, new york, ny 10005 made in the uk soapandglory.com
Information for Patients:
Information manufactured for the boots company plc nottingham england ng2 3aa. boots retail ireland dublin 12 ireland. dist. in the usa by boots retail usa, new york, ny 10005 made in the uk soapandglory.com
Package Label Principal Display Panel:
Carton carton sgspf30
Further Questions:
Questions usa: questions? 1-866-752-6687