NDC 66902-777 Cvs Health Arnica Blend Roll-on

Aloe Vera Leaf, Arnica Montana Flower, Calendula Officinalis Flowering Top, Bellis Perennis

NDC Product Code 66902-777

NDC Code: 66902-777

Proprietary Name: Cvs Health Arnica Blend Roll-on What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Aloe Vera Leaf, Arnica Montana Flower, Calendula Officinalis Flowering Top, Bellis Perennis What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 66902 - Natural Essentials, Inc.
    • 66902-777 - Cvs Health Arnica Blend Roll-on

NDC 66902-777-03

Package Description: 89 mL in 1 CONTAINER

NDC Product Information

Cvs Health Arnica Blend Roll-on with NDC 66902-777 is a a human over the counter drug product labeled by Natural Essentials, Inc.. The generic name of Cvs Health Arnica Blend Roll-on is aloe vera leaf, arnica montana flower, calendula officinalis flowering top, bellis perennis. The product's dosage form is gel and is administered via topical form.

Labeler Name: Natural Essentials, Inc.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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.

Cvs Health Arnica Blend Roll-on 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.

  • ALOE VERA LEAF 3 [hp_X]/89mL
  • ARNICA MONTANA FLOWER 1 [hp_X]/89mL
  • CALENDULA OFFICINALIS FLOWERING TOP 3 [hp_X]/89mL
  • BELLIS PERENNIS 4 [hp_X]/89mL

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)
  • ALCOHOL (UNII: 3K9958V90M)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)

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: Natural Essentials, Inc.
Labeler Code: 66902
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: 06-03-2019 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: 12-31-2020 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Cvs Health Arnica Blend Roll-on Product Label Images

Cvs Health Arnica Blend Roll-on 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

Active Ingredients

Aloe 3X
Arnica Montana 1X (11%)
Calendula Officinalis 3X
Bellis Perrenis 4X

Purpose

Joint Pain
Bruises & Muscle Soreness
Pain Relief
Sprains and Bruises

Uses*

Homeopathic remedy/medicine for the relief of minor aches, strains, bruises and sprains.

Warnings

For external use only
Flammable:Keep away from fire or flame

Stop Use And Ask A Doctor If

  • A rash or other adverse reaction occurs
  • Symptoms worsen or persist for more than 7 days

Children Under 12 - Ask Your Doctor

  • Avoid contact with eyes or mucus membranes
  • If pregnant or breast feeding, ask a physician before use

When Using This Product

  • Do not use with other topical products
  • Do not use on open wounds
  • If swallowed, seek professional help and contact Poison Control Center right away.

Adults And Children 12 Years And Older:

  • Apply & gently massage painful joints and muscles
  • Repeat as needed, no more than 4 times a day
  • Wash hands after each use with cold water
  • Store in a cool dry area - close cap tight

Other Information

Active ingredients are HPUS and manufactured according to homeopathic principles

Inactive Ingredients

De-ionized water, SD alcohol 40-2, Glycerin, Cellulose Gum, Potassium Sorbate, Sodium Benzoate.

* Please review the disclaimer below.

Previous Code
66902-700
Next Code
66902-800