Allergy Nasal Spray
NDC Package 70163-0020-2
Package Information
Allergy Nasal (adrenalinum, allium cepa, ambrosia artemisiaefolia, echinacea (angustifolia), gelsemium sempervirens, kali iodatum, sanguinaria canadensis, sticta pulmonaria) sprays is adults and children 12 years and older:■ Use 2 sprays in each nostril every 4 hours or as needed■ Consult a physician for use in children under 12 years of age. This formulation utilizes a spray delivery system. Marketed by Naturalcare, this product is identified by NDC 70163-0020.
Identification & Billing
Clinical Specifications
- Adrenergic alpha-Agonists - [MoA] (Mechanism of Action)
- Adrenergic beta-Agonists - [MoA] (Mechanism of Action)
- Allergens - [CS]
- Catecholamine - [EPC] (Established Pharmacologic Class)
- Catecholamines - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Vegetable Proteins - [CS]
- alpha-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
- beta-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 70163 - Naturalcare
- 70163-0020 - Allergy Nasal
- 70163-0020-2 - 1 BOTTLE, SPRAY in 1 CARTON / 24 mL in 1 BOTTLE, SPRAY (70163-0020-1)
- 70163-0020 - Allergy Nasal
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 70163-0020-2 identifies a specific commercial package of 1 bottle, spray in 1 carton / 24 ml in 1 bottle, spray (70163-0020-1) of Allergy Nasal, a human over the counter drug labeled by Naturalcare. This spray is formulated for oral use and contains ambrosia artemisiifolia whole; echinacea angustifolia whole; epinephrine; gelsemium sempervirens root; lobaria pulmonaria; onion; potassium iodide; sanguinaria canadensis root 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 Naturalcare on May 14, 2026. The current certification is valid through December 31, 2027.
How is this Naturalcare product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 70163002002. 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.