TRIHERBAL 3 [hp_X]/1

Arnica montana, Phytolacca decandra, Sanguinaria canadensis · CAPSULE · Spaus Inc.

No Recall History

Plain English

TRIHERBAL is a capsule containing arnica montana, phytolacca decandra, sanguinaria canadensis at 3 [hp_X]/1, taken oral. Manufactured by Spaus Inc..

Key Facts

Brand Name: TRIHERBAL
Generic Name: Arnica montana, Phytolacca decandra, Sanguinaria canadensis
NDC Code (Product): 71989-718
Manufacturer: Spaus Inc.
Strength: 3 [hp_X]/1
Dosage Form: CAPSULE
Route: ORAL
Marketing Status
Marketing Start: 01/01/2026

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses Temporarily relieves minor aches, pains, and inflammation due to: ▪ Headache ▪ Menstrual cramps ▪ Minor pain of arthritis ▪ Backache ▪ Neuralgia ▪ Temporarily reduces fever ▪ Toothache ▪ Muscular aches

Dosage & Administration

Directions: Adults and children 12 years and older: Swallow 1-2 capsules every 4 – 6 hours as needed. Children under 12 years: Consult a doctor.

Warnings

Warnings Stop and ask a doctor if symptoms persist for more than 3 days or worsen. If pregnant or breastfeeding, ask a healthcare professional before use. Keep out of reach of children. In case of overdose, seek medical help or contact Poison Control Center immediately.

Frequently Asked Questions

What is TRIHERBAL used for?

TRIHERBAL contains Arnica montana, Phytolacca decandra, Sanguinaria canadensis. It is a capsule taken oral. Consult your doctor for specific uses.

Is TRIHERBAL a controlled substance?

TRIHERBAL is not classified as a controlled substance by the DEA.

What is the generic name for TRIHERBAL?

The generic name for TRIHERBAL is Arnica montana, Phytolacca decandra, Sanguinaria canadensis. There are no other listed brand versions of Arnica montana, Phytolacca decandra, Sanguinaria canadensis.

What is the NDC code for TRIHERBAL 3 [hp_X]/1?

The NDC (National Drug Code) for TRIHERBAL 3 [hp_X]/1 is 71989-718, listed by Spaus Inc..

Product NDC

71989-718

Package NDC

71989-718-20

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)