Radical Rescue Morning Uva/uvb Defense Primer Broad Spectrum Spf 30 Universal Tint Mineral Sunscreen Lotion, Augmented
NDC Package 87631-0001-3
Package Information
Radical Rescue Morning Uva/uvb Defense Primer Broad Spectrum Spf 30 Universal Tint Mineral Sunscreen (radical rescue spf 30 mineral sunscreen) lotions is uSES • helps prevent sunburn • If used as directed with other sun protection measures (see Directions),decreases the risk of skin cancer, and early skin agingcaused by the sun. This formulation utilizes a lotion, augmented delivery system. Marketed by Protransit, Inc., this product is identified by NDC 87631-0001 and is authorized under FDA application M020.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 87631 - Protransit, Inc.
- 87631-0001 - Radical Rescue Morning Uva/uvb Defense Primer Broad Spectrum Spf 30 Universal Tint Mineral Sunscreen
- 87631-0001-3 - 1 POUCH in 1 CARTON / 1 mL in 1 POUCH (87631-0001-2)
- 87631-0001 - Radical Rescue Morning Uva/uvb Defense Primer Broad Spectrum Spf 30 Universal Tint Mineral Sunscreen
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.
* 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 87631-0001-3 identifies a specific commercial package of 1 pouch in 1 carton / 1 ml in 1 pouch (87631-0001-2) of Radical Rescue Morning Uva/uvb Defense Primer Broad Spectrum Spf 30 Universal Tint Mineral Sunscreen, a human over the counter drug labeled by Protransit, Inc.. This lotion, augmented is formulated for topical use and contains zinc oxide; 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 Protransit, Inc. on July 15, 2026. The current certification is valid through December 31, 2027.
How is this Protransit, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 87631000103. 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.