A-12 Solution
NDC Package 58264-0304-1
Package Information
A-12 (juniperus ashei pollen, juniperus virginiana pollen, tamarix gallica pollen, cupressus arizonica pollen, taxodium distichum pollen, juniperus monosperma pollen, juniperus pinchotii pollen, juniperus scopulorum pollen, pinus taeda pollen, pinus strobus pollen, and pinus echinata pollen) solution is a medication used as Allergies. This formulation utilizes a solution delivery system. Marketed by Dna Labs, Inc., this product is identified by NDC 58264-0304.
Identification & Billing
Clinical Specifications
- CUPRESSUS ARIZONICA POLLEN 30 [hp_X]/mL
- JUNIPERUS ASHEI POLLEN 30 [hp_X]/mL
- JUNIPERUS MONOSPERMA POLLEN 30 [hp_X]/mL
- JUNIPERUS PINCHOTII POLLEN 30 [hp_X]/mL
- JUNIPERUS SCOPULORUM POLLEN 30 [hp_X]/mL
- JUNIPERUS VIRGINIANA POLLEN 30 [hp_X]/mL
- PINUS ECHINATA POLLEN 30 [hp_X]/mL
- PINUS STROBUS POLLEN 30 [hp_X]/mL
- PINUS TAEDA POLLEN 30 [hp_X]/mL
- TAMARIX GALLICA POLLEN 30 [hp_X]/mL
- TAXODIUM DISTICHUM POLLEN 30 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 58264 - Dna Labs, Inc.
- 58264-0304 - A-12
- 58264-0304-1 - 29.57 mL in 1 BOTTLE, GLASS
- 58264-0304 - A-12
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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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 58264-0304-1 identifies a specific commercial package of 29.57 ml in 1 bottle, glass of A-12, a human over the counter drug labeled by Dna Labs, Inc.. This solution is formulated for sublingual use and contains cupressus arizonica pollen; juniperus ashei pollen; juniperus monosperma pollen; juniperus pinchotii pollen; juniperus scopulorum pollen; juniperus virginiana pollen; pinus echinata pollen; pinus strobus pollen; pinus taeda pollen; tamarix gallica pollen; taxodium distichum pollen 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 Dna Labs, Inc. on January 01, 1990. The current certification is valid through December 31, 2026.
How is this Dna Labs, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 58264030401. 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.