NDC 82312-001 Arthroneo


NDC Product Code 82312-001

NDC 82312-001-50

Package Description: 1 BOTTLE, SPRAY in 1 BOX > 50 g in 1 BOTTLE, SPRAY

NDC Product Information

Arthroneo with NDC 82312-001 is a a human over the counter drug product labeled by Likasso Ltd. The generic name of Arthroneo is camphor. The product's dosage form is spray and is administered via topical form.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Arthroneo 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.

  • LINALOOL, (+)- (UNII: F4VNO44C09)
  • WATER (UNII: 059QF0KO0R)
  • LIMONENE, (+)- (UNII: GFD7C86Q1W)

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: Likasso Ltd
Labeler Code: 82312
FDA Application Number: part348 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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: 10-27-2021 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.

Arthroneo 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 Ingredient

Camphor 0.50%


External Analgesic


For temporary relief of pain


For external use only.

Do Not Use

In large quantities, particularly over raw surfaces or blistered areas.• If condition worsens or if symptoms persist for more than 7 days or clear up and ocur again within a few days, discontinue use of this product and consult a doctor.

When Using This Product

Avoid contact with the eyes

Stop Using And Ask A Doctor

If irritation or rash occurs.

Keep Out Of Reach Of Children

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


Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age:

consult a doctor.

Other Information

Keep dry. Store at 5'C and 20'C.

Inactive Ingredients

Sensil CH SP, Amica montana flower extract, Benzyl alcohol, Citric acid, Disodium EDTA, Limonene, Lavandula angustifolia herb oil,

Linalool, Peg-40 hydrogenated castor oil, Potassium sorbate, Propylene glycol, Sodium benzoate, Water

Principal Display

Made in the EUManufacturered for Likasso, LTDGrafenberger Alle 1154023 Dusseldorf, GermanyNDC: 82312-001-50

* Please review the disclaimer below.