Cvs Health Arnica Blend Roll-on

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

Natural Essentials, Inc.
Human Otc Drug
NDC 66902-777

Cvs Health Arnica Blend Roll-on also known as Aloe Vera Leaf, Arnica Montana Flower, Calendula Officinalis Flowering Top, Bellis Perennis Whole is a human otc drug labeled by 'Natural Essentials, Inc.'. National Drug Code (NDC) number for Cvs Health Arnica Blend Roll-on is 66902-777. This drug is available in dosage form of Gel. The names of the active, medicinal ingredients in Cvs Health Arnica Blend Roll-on drug includes Aloe Vera Leaf - 3 [hp_X]/89mL Arnica Montana Flower - 1 [hp_X]/89mL Bellis Perennis Whole - 4 [hp_X]/89mL Calendula Officinalis Flowering Top - 3 [hp_X]/89mL . The currest status of Cvs Health Arnica Blend Roll-on drug is Active.

Drug Information:

Drug NDC:	66902-777
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Cvs Health Arnica Blend Roll-on
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Aloe Vera Leaf, Arnica Montana Flower, Calendula Officinalis Flowering Top, Bellis Perennis Whole
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Natural Essentials, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Gel
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ALOE VERA LEAF - 3 [hp_X]/89mL ARNICA MONTANA FLOWER - 1 [hp_X]/89mL BELLIS PERENNIS WHOLE - 4 [hp_X]/89mL CALENDULA OFFICINALIS FLOWERING TOP - 3 [hp_X]/89mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	TOPICAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	03 Jun, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	08 May, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	NATURAL ESSENTIALS, INC.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
UPC:	0050428578230
UPC stands for Universal Product Code.
UNII:	ZY81Z83H0X OZ0E5Y15PZ 2HU33I03UY 18E7415PXQ
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
66902-777-03	89 mL in 1 CONTAINER (66902-777-03)	03 Jun, 2019	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Cvs Health Arnica Blend Roll-on

Aloe Vera Leaf & more..

Gel
NATURAL ESSENTIALS, INC.
NDC: 66902-777

Purpose:

Purpose joint pain bruises & muscle soreness pain relief sprains and bruises

Product Elements:

Cvs health arnica blend roll-on aloe vera leaf, arnica montana flower, calendula officinalis flowering top, bellis perennis whole aloe vera leaf aloe vera leaf arnica montana flower arnica montana flower calendula officinalis flowering top calendula officinalis flowering top bellis perennis whole bellis perennis whole water alcohol glycerin carboxymethylcellulose sodium, unspecified potassium sorbate sodium benzoate

Indications and Usage:

Uses* homeopathic remedy/medicine for the relief of minor aches, strains, bruises and sprains.

Warnings:

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.

When Using:

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.

Dosage and Administration:

Directions 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

Stop Use:

Stop use and ask a doctor if a rash or other adverse reaction occurs symptoms worsen or persist for more than 7 days

Package Label Principal Display Panel:

Principal display panel - arnica blend roll-on cvs health â¢ arnica blend roll-on aloe - joint pain* arnica montana - bruises & muscle soreness* calendula officinalis - pain relief* bellis perrenis - sprains & bruises* relief for pain, stiffness & swelling* homeopathic absorbs quickly fragrance free non-greasy 3 fl oz (89 ml) *claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated. principal display panel - arnica blend roll-on

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.