Arnicare Bruise 1 [hp_X]/g

ARNICA MONTANA · GEL · Laboratoires Boiron

No Recall History

Plain English

Arnicare Bruise is a gel containing arnica montana at 1 [hp_X]/g, taken topical. Manufactured by Laboratoires Boiron.

Key Facts

Brand Name: Arnicare Bruise
Generic Name: ARNICA MONTANA
NDC Code (Product): 0220-9084
Manufacturer: Laboratoires Boiron
Strength: 1 [hp_X]/g
Dosage Form: GEL
Route: TOPICAL
Marketing Status
Marketing Start: 02/01/2016

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses* reduces symptoms of bruising such as: minor pain swelling discoloration

Dosage & Administration

Directions Adults and children 1 year of age and older: Apply a thin layer of Arnicare Bruise Gel to affected area and massage gently as soon as possible after minor bruise up to 3 times a day. If heat or ice is applied, wait 5 minutes before applying Arnicare Bruise Gel. Children under 1 year of age: Not recommended.

Warnings

Warnings For external use only.

Frequently Asked Questions

What is Arnicare Bruise used for?

Arnicare Bruise contains ARNICA MONTANA. It is a gel taken topical. Consult your doctor for specific uses.

Is Arnicare Bruise a controlled substance?

Arnicare Bruise is not classified as a controlled substance by the DEA.

What is the generic name for Arnicare Bruise?

The generic name for Arnicare Bruise is ARNICA MONTANA. There are 12 other brand versions of ARNICA MONTANA.

What is the NDC code for Arnicare Bruise 1 [hp_X]/g?

The NDC (National Drug Code) for Arnicare Bruise 1 [hp_X]/g is 0220-9084, listed by Laboratoires Boiron.

Product NDC

0220-9084

Package NDC

0220-9084-54

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

Data from openFDA · Public domain (CC0 1.0)