Stress Away Anxiety Relief Spray
NDC Package 68703-349-02
Package Information
Stress Away Anxiety Relief (aconitum nap, alfalfa, avena, chamomilla, gelsemium, humulus lupulus, ignatia, kali ars, kali phos, muriaticum ac, nat phos, passiflora, phos, staphysag, stramonium) sprays is directions: Initially, depress pump until primed. This formulation utilizes a spray delivery system. Marketed by Silver Star Brands, this product is identified by NDC 68703-349.
Identification & Billing
Clinical Specifications
- ACONITUM NAPELLUS 10 [hp_X]/59mL
- ALFALFA 10 [hp_X]/59mL
- AVENA SATIVA LEAF 10 [hp_X]/59mL
- DATURA STRAMONIUM 10 [hp_X]/59mL
- DELPHINIUM STAPHISAGRIA SEED 10 [hp_X]/59mL
- GELSEMIUM SEMPERVIRENS ROOT 10 [hp_X]/59mL
- HUMULUS LUPULUS WHOLE 10 [hp_X]/59mL
- HYDROCHLORIC ACID 10 [hp_X]/59mL
- MATRICARIA CHAMOMILLA FLOWERING TOP OIL 10 [hp_X]/59mL
- PASSIFLORA INCARNATA FLOWERING TOP 10 [hp_X]/59mL
- PHOSPHORUS P-32 10 [hp_X]/59mL
- POTASSIUM ARSENITE ANHYDROUS 10 [hp_X]/59mL
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM 10 [hp_X]/59mL
- SODIUM PHOSPHATE, DIBASIC 10 [hp_X]/59mL
- STRYCHNOS IGNATII WHOLE 10 [hp_X]/59mL
Regulatory & Marketing
Hierarchy Structure
- 68703 - Silver Star Brands
- 68703-349 - Stress Away Anxiety Relief
- 68703-349-02 - 59 mL in 1 BOTTLE, SPRAY
- 68703-349 - Stress Away Anxiety Relief
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 68703-349-02 identifies a specific commercial package of 59 ml in 1 bottle, spray of Stress Away Anxiety Relief, a human over the counter drug labeled by Silver Star Brands. This spray is formulated for oral use and contains aconitum napellus; alfalfa; avena sativa leaf; datura stramonium; delphinium staphisagria seed; gelsemium sempervirens root; humulus lupulus whole; hydrochloric acid; matricaria chamomilla flowering top oil; passiflora incarnata flowering top; phosphorus p-32; potassium arsenite anhydrous; potassium phosphate, unspecified form; sodium phosphate, dibasic; strychnos ignatii whole 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 Silver Star Brands on October 01, 2019. The current certification is valid through December 31, 2026.
How is this Silver Star Brands product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 68703034902. Quantities are measured in C112160. 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 Product segment to maintain the 5-4-2 structure.