Bruiseguard Md
FDA Label NDC 64269-9910

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Scarguard Labs, Llc for the product Bruiseguard Md (NDC 64269-9910). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, keep out of reach of children, directions, inactive ingredients, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Arnica 1m
Arnica 30c

Purpose

Anti-bruising

Anti-bruising

Uses

to clear/fade appearance of bruises

Warnings

  • for adult use only
  • keep out of reach of children
  • do not exceed daily dosage
  • do not use with Talwin
  • do not use with blood thinners unless instructed by your doctor

Keep Out Of Reach Of Children

If swallowed by children, get medical help or contact a Poison Control Center right away.

Directions

  • use one dosage card per day
  • follow daily sequence of dosage cards
  • take tablets from card three times per day
  • arnica tablets to be placed under tongue to dissolve
  • for best results take on empty stomach

Inactive Ingredients

Lactose, Sorbitol, Silicone Dioxide, Crospovidone

Otc - Questions

call 1-877-566-5935

Bruiseguard Md Carton

Bruiseguard Md Carton (Bruiseguardmd)

Bruiseguard Md Carton (Bruiseguardmd)

* Please review the disclaimer below.