By Selected Daily Broad Spectrum Sunscreen
Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate
Garam Of Nature
Human Otc Drug
NDC 73509-050By Selected Daily Broad Spectrum Sunscreen also known as Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate is a human otc drug labeled by 'Garam Of Nature'. National Drug Code (NDC) number for By Selected Daily Broad Spectrum Sunscreen is 73509-050. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in By Selected Daily Broad Spectrum Sunscreen drug includes Octinoxate - 3.5 g/50mL Octisalate - 2 g/50mL . The currest status of By Selected Daily Broad Spectrum Sunscreen drug is Active.
Drug Information:
| Drug NDC: | 73509-050 |
| 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: | By Selected Daily Broad Spectrum Sunscreen |
| 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: | Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Garam Of Nature |
| 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: | OCTINOXATE - 3.5 g/50mL
OCTISALATE - 2 g/50mL
|
| 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: | UNAPPROVED DRUG OTHER |
| 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 Jul, 2021 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 22 Dec, 2025 |
| 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. |
| 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: | Garam Of Nature
|
| 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: | 4Y5P7MUD51
4X49Y0596W
|
| 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 |
|---|
| 73509-050-02 | 1 TUBE in 1 CARTON (73509-050-02) / 50 mL in 1 TUBE (73509-050-01) | 01 Jul, 2021 | 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
Product Elements:
By selected daily broad spectrum sunscreen ethylhexyl methoxycinnamate, ethylhexyl salicylate octinoxate octinoxate octisalate octisalate water dipropylene glycol
Indications and Usage:
Uses â helps prevent sunburn â it used as directed with other sun protection measures (see directions). decreases the risk of skin cancer and early skin aging caused by the sun
Warnings:
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 occurs keep out of reach of children. if product is swallowed, get medical help or contact a posion control center right away
Dosage and Administration:
Directions â apply liberally and spread evenly by hand 15 minutes before sun exposureâ¢reapply:â¢after 80 minutes of swimming or sweatingâ¢immediately after towel drying ⢠at least every 2 hoursâ¢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 of 15 or higher and other sun protection measures including: ⢠limit time in the sun, especially from 10 a.m. â 2 p.m. ⢠wear long-sleeve shirts, pants, hats, and sunglasses ⢠children under 6 months: ask a docto
Package Label Principal Display Panel:
Package label.principal display panel image of carton
Further Questions:
Questions www.byselected.co.kr byselected@naver.com +82-70-8883-2525