Valerin Tablet
NDC Package 99528-606-06

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

Package Information

Valerin (valerian root, passiflora, magnesium carbonate) tablets is when Using This Product: Avoid contact with eyes or mucous membranes- Do not apply to wounds or damaged skin - Do not use with other ointments, creams, sprays or liniments - Do not apply to irritated skin or if excessive irritation develops - Do not bandage - Wash hands after use with cool water - Do not use with heating pad or heating devices. This formulation utilizes a tablet delivery system. Marketed by Wonder Laboratories, this product is identified by NDC 99528-606.

Identification & Billing

NDC Package Code
99528-606-06
Package Description
6 TABLET in 1 BAG
Product Code
11-Digit Billing Format
99528060606

Clinical Specifications

Proprietary Name
Valerin
Non-Proprietary Name
Valerian Root, Passiflora, Magnesium Carbonate
Substance Name
Magnesium Carbonate; Passiflora Incarnata Flower; Valerian
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
When Using This Product: Avoid contact with eyes or mucous membranes- Do not apply to wounds or damaged skin - Do not use with other ointments, creams, sprays or liniments - Do not apply to irritated skin or if excessive irritation develops - Do not bandage - Wash hands after use with cool water - Do not use with heating pad or heating devices

Regulatory & Marketing

Labeler Name
Wonder Laboratories
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
06-12-1986
Listing Expiration
12-31-2026
Exclude Flag
N
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (99528-606). Click a package code to view its specific billing and regulatory data.

12 TABLET in 1 BAG
250 TABLET in 1 BOTTLE
45 TABLET in 1 BOTTLE
90 TABLET in 1 BOTTLE

* 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 99528-606-06 identifies a specific commercial package of 6 tablet in 1 bag of Valerin, a human over the counter drug labeled by Wonder Laboratories. This tablet is formulated for oral use and contains magnesium carbonate; passiflora incarnata flower; valerian 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 Wonder Laboratories on June 12, 1986. The current certification is valid through December 31, 2026.

How is this Wonder Laboratories product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 99528060606. 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)
99528-606-06
11-Digit CMS (5-4-2)
99528-0606-06

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