Bo Spf15
NDC Package 59735-100-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Bo Spf15 is apply liberally 15 minutes before sun exposureUse water resistant sunscreen if swimming or sweathingReapply at least every 2 hoursChildren under 6 months: ask a doctorSun Protection Measures: Spending time in the sun decreases risk of skin cancer and early again. Marketed by Mana Products, this product is identified by NDC 59735-100 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
59735-100-01
Package Description
75 g in 1 TUBE
Product Code
59735-100
11-Digit Billing Format
59735010001

Clinical Specifications

Proprietary Name
Bo Spf15
Dosage Form
-
Usage Information
Apply liberally 15 minutes before sun exposureUse water resistant sunscreen if swimming or sweathingReapply at least every 2 hoursChildren under 6 months: ask a doctorSun Protection Measures: Spending time in the sun decreases risk of skin cancer and early again. To decrease this risk, regulaory 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 10:00 am - 2:00 pm. Wear long sleeved shirts, pants, hats and sunglasses.

Regulatory & Marketing

Labeler Name
Mana Products
FDA Application #
part352
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
09-27-2013
Listing Expiration
12-31-2019
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 59735-100-01 identifies a specific commercial package of 75 g in 1 tube of Bo Spf15, labeled by Mana Products. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Mana Products on September 27, 2013. The current certification is valid through December 31, 2019.

How is this Mana Products product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 59735010001. 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:

10-Digit Format (5-3-2)
59735-100-01
11-Digit CMS (5-4-2)
59735-0100-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.