PTS/Stress Remedy NDC 43742-1322

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1322Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1322Add 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
43742-1322-1	43742132201	30 mL in 1 BOTTLE, DROPPER (43742-1322-1)Marketed from Aug 28, 2018

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): PTS/Stress Remedy
Generic name (nonproprietary): kali phosphoricum, ambra grisea, cacao, phosphoricum acidum, arnica montana, calcarea carbonica, cerebrum suis, glandula suprarenalis suis, lithium carbonicum, aconitum napellus, argemone mexicana, arsenicum album, cicuta virosa, hyoscyamus niger, ignatia tigrinum, natrum muriaticum, tarentula hispanica, stramonium, buthus australis
Active ingredients: Dibasic potassium phosphate — 3 [hp_X]/mLAmbergris — 6 [hp_X]/mLCocoa — 6 [hp_X]/mLPhosphoric acid — 6 [hp_X]/mLArnica montana — 6 [hp_X]/mLOyster shell calcium carbonate, Crude — 8 [hp_X]/mLSus scrofa cerebrum — 8 [hp_X]/mLSus scrofa adrenal gland — 8 [hp_X]/mLLithium carbonate — 8 [hp_X]/mLAconitum napellus — 8 [hp_X]/mLArgemone mexicana — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLCicuta virosa root — 12 [hp_X]/mLHyoscyamus niger — 12 [hp_X]/mLStrychnos ignatii seed — 12 [hp_X]/mLLilium lancifolium whole flowering — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLLycosa tarantula — 12 [hp_X]/mLDatura stramonium — 12 [hp_X]/mLAndroctonus australis venom — 6 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 28, 2018
Marketing end: Dec 28, 2028
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 43742-1322_57eaf84a-12fd-4a9d-b4ff-68e78f5ca2b9SPL ID 57eaf84a-12fd-4a9d-b4ff-68e78f5ca2b9SPL set ID 05341147-789a-4844-9412-6a3044e5eb18UNII CI71S98N1Z, XTC0D02P6C, D9108TZ9KG, E4GA8884NN, O80TY208ZW, 2E32821G6I, 4GB5DQR532, 398IYQ16YV, 2BMD2GNA4V, U0NQ8555JD, 6X68976407, S7V92P67HO, YEA9P21S8N, 4WRK2153H3, 1NM3M2487K, X67Z2963PI, 451W47IQ8X, 86M454L2TT, G6W4F0V8Z3, 25IMQ489AW
Pharmacologic class: Mood Stabilizer; Non-Standardized Food Allergenic Extract

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

N443742132201 followed by a unit qualifier and the quantity

Package 43742-1322-01. 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 Mar 4, 2024.

Indications (excerpt from the label)

HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms of stress such as terror, horror, post traumatic stress, fight or flight response, recurring nightmares, difficulty sleeping, difficulty concentrating, restlessness, and easy irritability.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)