Banana Boat Baby Tear Free Lotion Spf 50
NDC Package 17630-2006-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

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

Banana Boat Baby Tear Free Lotion Spf 50 is shake well before use. Marketed by Accra-pac, Inc., this product is identified by NDC 17630-2006 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
17630-2006-1
Package Description
180 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
17630200601

Clinical Specifications

Proprietary Name
Banana Boat Baby Tear Free Lotion Spf 50
Dosage Form
-
Usage Information
Shake well before use. Apply generously and evenly to all areas 20 minutes before sun exposure. Do not spray directly on face. Spray on hands to apply to face. Reapply at frequent intervals, after swimming, towel drying and perspiring. For external use only. Avoid contact with eyes and fabrics.

Regulatory & Marketing

Labeler Name
Accra-pac, Inc.
FDA Application #
part352
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
07-23-2009
Listing Expiration
12-31-2018
Exclude Flag
I
Sample Package
No

Hierarchy Structure

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 17630-2006-1 identifies a specific commercial package of 180 ml in 1 bottle of Banana Boat Baby Tear Free Lotion Spf 50, labeled by Accra-pac, Inc.. 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 Accra-pac, Inc. on July 23, 2009. The current certification is valid through December 31, 2018.

How is this Accra-pac, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 17630200601. 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 (5-4-1)
17630-2006-1
11-Digit CMS (5-4-2)
17630-2006-01

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