Active Ingredient
Arnica Montana 1X HPUS 7%.
Iqvppw Arnica Bruise Cream
FDA Label NDC 87786-069
13 label sections · Submitted to the FDA by Wenzhou Yuyuan Pharmaceutical Co., Ltd. · Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Wenzhou Yuyuan Pharmaceutical Co., Ltd. for the product Iqvppw Arnica Bruise Cream (NDC 87786-069). 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 ingredient, purpose, uses, warnings, do not use, when using, stop use, ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Bruising & Pain Relief
Uses
·Temporarily relieves pain, swelling, and discoloration associated with bruises,minor injuries, muscle soreness, and bumps.
Warnings
For external use only.
Do Not Use
·Do not use on broken skin
When Using
·Avoid contact with eyes
Stop Use
·Stop use and ask a doctor if condition persists for more than 3 days or worsens,or if symptoms clear up and occur again within a few days.
Ask Doctor
·Stop use and ask a doctor if condition persists for more than 3 days or worsens,or if symptoms clear up and occur again within a few days.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Apply a thin layer of cream to the affected area as soon as possible after minor injury.
·Repeat 3 times a day as needed.
·If heat or ice is applied, wait 5 minutes before applying cream.
Other Information
·Store at 20°-25°C(68°-77°F)
Inactive Ingredients
Alcohol, carbomer, purified water,Arnica, sodium hydroxide,Vitamin B₆, VitaminE, Vanillyl butyl ether, Msm, Aloe vera
Principal Display Panel
7 (C342c157308b22d8aeffef4e42c4fe34)
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