Stress Away Anxiety Relief NDC 68703-349

NDC codes

FDA NDC Directory

Product NDC (as listed)68703-349Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68703-0349Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
68703-349-02	68703034902	59 mL in 1 BOTTLE, SPRAY (68703-349-02)Marketed from Oct 1, 2019

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Stress Away Anxiety Relief
Generic name (nonproprietary): aconitum nap, alfalfa, avena, chamomilla, gelsemium, humulus lupulus, ignatia, kali ars, kali phos, muriaticum ac, nat phos, passiflora, phos, staphysag, stramonium
Active ingredients: Hydrochloric acid — 10 [hp_X]/59mLPhosphorus p-32 — 10 [hp_X]/59mLDatura stramonium — 10 [hp_X]/59mLDelphinium staphisagria seed — 10 [hp_X]/59mLAlfalfa — 10 [hp_X]/59mLMatricaria chamomilla flowering top oil — 10 [hp_X]/59mLPotassium phosphate, Unspecified form — 10 [hp_X]/59mLSodium phosphate, Dibasic — 10 [hp_X]/59mLAconitum napellus — 10 [hp_X]/59mLGelsemium sempervirens root — 10 [hp_X]/59mLHumulus lupulus whole — 10 [hp_X]/59mLStrychnos ignatii whole — 10 [hp_X]/59mLPotassium arsenite anhydrous — 10 [hp_X]/59mLPassiflora incarnata flowering top — 10 [hp_X]/59mLAvena sativa leaf — 10 [hp_X]/59mL
Dosage form: Spray
Route: Oral
Labeler: Silver Star Brands
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 1, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)
Identifiers: Product ID 68703-349_2868834b-60c7-edec-e063-6394a90ac040SPL ID 2868834b-60c7-edec-e063-6394a90ac040SPL set ID 9d75666e-3214-2bab-e053-2a95a90af719UNII QTT17582CB, 690284A407, G6W4F0V8Z3, 00543AP1JV, DJO934BRBD, SA8AR2W4ER, B7862WZ632, GR686LBA74, U0NQ8555JD, 639KR60Q1Q, 912A6Q1N4A, 6YSJ329777, BM2U42PAKI, CLF5YFS11O, 206PI19V7RUPC 0818837015339
Pharmacologic class: Osmotic Laxative

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468703034902 followed by a unit qualifier and the quantity

Package 68703-0349-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Dec 3, 2024.

Indications (excerpt from the label)

Uses* Uses*: Temporarily relieves minor anxiousness and nervousness.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)