TremorSoothe NDC 68703-352

NDC codes

FDA NDC Directory

Product NDC (as listed)68703-352Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68703-0352Add 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
68703-352-80	68703035280	189 TABLET in 1 BOTTLE, GLASS (68703-352-80)Marketed from Dec 25, 2020

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): TremorSoothe
Generic name (nonproprietary): agaricus musc, mag phos, stramonium, tarentula hisp
Active ingredients: Amanita muscaria fruiting body — 6 [hp_C]/1801Magnesium phosphate, Dibasic trihydrate — 8 [hp_X]/1801Lycosa tarantula — 6 [hp_C]/1801Datura stramonium — 6 [hp_C]/1801
Dosage form: Tablet
Route: Oral
Labeler: Silver Star Brands
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 25, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 68703-352_2ab1287c-c753-6a71-e063-6394a90a1cddSPL ID 2ab1287c-c753-6a71-e063-6394a90a1cddSPL set ID b6c17f42-6a08-6f89-e053-2a95a90aafaaUNII DIF093I037, HF539G9L3Q, 86M454L2TT, G6W4F0V8Z3UPC 0810845016414
Pharmacologic class: Calculi Dissolution Agent; 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

N468703035280 followed by a unit qualifier and the quantity

Package 68703-0352-80. 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 Jan 1, 2025.

Indications (excerpt from the label)

Uses*: Uses*: Homeopathic remedy for temporary relief of dizziness and nausea. *Clais based on traditional homeopatchi practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)