Soleo Organics Sunscreen
Zinc Oxide
Se Operations Pty Ltd
Human Otc Drug
NDC 11045-0303Soleo Organics Sunscreen also known as Zinc Oxide is a human otc drug labeled by 'Se Operations Pty Ltd'. National Drug Code (NDC) number for Soleo Organics Sunscreen is 11045-0303. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in Soleo Organics Sunscreen drug includes Zinc Oxide - 223 mg/g . The currest status of Soleo Organics Sunscreen drug is Active.
Drug Information:
| Drug NDC: | 11045-0303 |
| 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: | Soleo Organics 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: | Zinc Oxide |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Se Operations Pty 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: | ZINC OXIDE - 223 mg/g
|
| 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: | 20 Jan, 2007 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 14 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: | SE Operations Pty 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: | SOI2LOH54Z
|
| 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 |
|---|
| 11045-0303-1 | 40 g in 1 TUBE (11045-0303-1) | 20 Jan, 2007 | N/A | No |
| 11045-0303-2 | 1 TUBE in 1 CARTON (11045-0303-2) / 80 g in 1 TUBE | 20 Jan, 2007 | N/A | No |
| 11045-0303-3 | 1 TUBE in 1 CARTON (11045-0303-3) / 150 g in 1 TUBE | 20 Jan, 2007 | 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:
Soleo organics sunscreen zinc oxide zinc oxide zinc oxide grape seed oil sunflower oil medium-chain triglycerides candelilla wax yellow wax macadamia oil theobroma grandiflorum seed butter green tea leaf chamaemelum nobile flower lecithin, soybean safflower oil cucumber .alpha.-tocopherol
Indications and Usage:
Uses helps prevent sunburn higher spf gives more sunburn protection provides high protection against sunburn retains spf after 80 minutes of activity in the water
Warnings:
Warnings for external use only when using this product keep out of eyes, rinse with water to remove keep out of reach of children avoid prolonged exposure to the sun wear protective clothing, hats and eye wear when in the sun stop use and ask a doctor if rash or irritation develops and lasts
When Using:
When using this product keep out of eyes, rinse with water to remove
Dosage and Administration:
Directions squeeze cream and shake tube well before use apply liberally 20 minutes before sun exposure and as needed store below 30°c/86°f
Package Label Principal Display Panel:
Principal display panel - 80 g tube carton multi award winning # 1 sunscreen soléo ® organics original formula high performance ⢠se formula ⢠se formula all natural sunscreen spf 30 3hour very water resistant* uv-a uv-b broad spectrum 80g/2.8 oz e aust-l 116246 principal display panel - 80 g tube carton