Brush And Go Spf 50 Powder
NDC Package 78863-3003-2
Package Information
Brush And Go Spf 50 (titanium dioxide, octinoxate, octocrylene, octisalate, avobenzone, and oxybenzone) powders is apply liberally 15 minutes before sun exposure and as needed.Use a water-resistant sunscreen if swimming or sweating.Reapply at least every 2 hours.Children under 6 months: Ask a doctor.Sun Protection Measures.Spending time in the sun increases your risk of skin cancer and early skin aging. This formulation utilizes a powder delivery system. Marketed by Noon Aesthetics M.r. Ltd, this product is identified by NDC 78863-3003 and is authorized under FDA application M020.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 78863 - Noon Aesthetics M.r. Ltd
- 78863-3003 - Brush And Go Spf 50
- 78863-3003-2 - 3 BOTTLE, PLASTIC in 1 CARTON / 5 mL in 1 BOTTLE, PLASTIC
- 78863-3003 - Brush And Go Spf 50
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Other Available Packages
The following commercial packages are registered under the same Product NDC (78863-3003). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 78863-3003-2 identifies a specific commercial package of 3 bottle, plastic in 1 carton / 5 ml in 1 bottle, plastic of Brush And Go Spf 50 All Skin Types Broad Spectrum, a human over the counter drug labeled by Noon Aesthetics M.r. Ltd. This powder is formulated for topical use and contains avobenzone; octinoxate; octisalate; octocrylene; oxybenzone; titanium dioxide as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Noon Aesthetics M.r. Ltd on April 01, 2024. The current certification is valid through December 31, 2027.
How is this Noon Aesthetics M.r. Ltd product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 78863300302. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.