NDC 0220-9055 Arnicare Foot Care

Arnica Montana

NDC Product Code 0220-9055

NDC 0220-9055-82

Package Description: 1 TUBE in 1 PACKAGE > 1 [hp_X] in 1 TUBE

NDC Product Information

Arnicare Foot Care with NDC 0220-9055 is a a human over the counter drug product labeled by Boiron. The generic name of Arnicare Foot Care is arnica montana. The product's dosage form is cream and is administered via topical form.

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Arnicare Foot Care Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • CARBOMER 934 (UNII: Z135WT9208)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Boiron
Labeler Code: 0220
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 06-01-2018 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Arnicare Foot Care Product Label Images

Arnicare Foot Care Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Arnica montana 1X HPUS 7%

Indications & Usage

Foot Pain ReliefFoot, ankle, arch, and heel painSore and aching feetSwelling from strains and sprainsJoint pain

Otc - Do Not Use

Do not use if glued carton end flaps are open or if tube seal is broken

Dosage & Administration

Apply a thin layer of Arnicare Foot Care to affected area and massage gently 3 times a day or as needed. If heat or ice is applied, wait five minutes before applying Arnicare Foot Care.

Inactive Ingredient

Alcohol, caprylyl glycol, carbomer, cetyl palmitate, glycerin, lauroyl macrogolglycerides, pexoxol-7 stearate, purified water, sodium hydroxide, sorbic acid, 1,2-hexanediol

How Supplied

4.2 oz tube (120g)

Otc - Purpose

Relieves pain and soreness, swelling from injuries, discoloration from bruises

Storage And Handling

Store at 68-77F (20-25C)

Otc - Questions

[email protected](1-800-264-7661)Distributed by Boiron Inc.6 Campus Blvd.Newtown Square, PA 19073-3267

Otc - Stop Use

Stop use and ask a doctor if condition persists for more than 3 days or worsens.

Otc - When Using

When using this product-use only as directed, do not tightly wrap or bandage the treated area, do not apply heat or ice to the treated area immediately before or after use


For external use only, avoid contact with eyes, mucous membranes, wounds or damaged or irritated skinIf swallowed, get medical help or contact a Poison Control Center right away.

* Please review the disclaimer below.