NDC 24909-745 Cbdmedic Back And Neck Pain Relief

Camphor And Menthol

NDC Product Code 24909-745

NDC 24909-745-02

Package Description: 1.7 g in 1 PACKET

NDC 24909-745-04

Package Description: 2 PACKET in 1 BLISTER PACK > 1.7 g in 1 PACKET

NDC 24909-745-07

Package Description: 1 TUBE in 1 BLISTER PACK > 7 g in 1 TUBE

NDC 24909-745-40

Package Description: 1 TUBE in 1 CARTON > 40 g in 1 TUBE

NDC Product Information

Cbdmedic Back And Neck Pain Relief with NDC 24909-745 is a a human over the counter drug product labeled by Aidance Skincare & Topical Solutions, Llc. The generic name of Cbdmedic Back And Neck Pain Relief is camphor and menthol. The product's dosage form is ointment and is administered via topical form.

Dosage Form: Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >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.

Cbdmedic Back And Neck Pain Relief 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.

  • WHITE WAX (UNII: 7G1J5DA97F)
  • CLOVE OIL (UNII: 578389D6D0)
  • COTTONSEED OIL (UNII: H3E878020N)
  • EUCALYPTUS OIL (UNII: 2R04ONI662)
  • HEMP (UNII: TD1MUT01Q7)
  • JOJOBA OIL (UNII: 724GKU717M)
  • PEPPERMINT OIL (UNII: AV092KU4JH)
  • SORBIC ACID (UNII: X045WJ989B)
  • TEA TREE OIL (UNII: VIF565UC2G)

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: Aidance Skincare & Topical Solutions, Llc
Labeler Code: 24909
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: 09-01-2019 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: 12-31-2021 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.

Cbdmedic Back And Neck Pain Relief Product Label Images

Cbdmedic Back And Neck Pain Relief 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 And Purpose

Camphor 10%, Menthol 15% (External Analgesics)

Uses

Temporary relief of minor aches and pains of muscles and joints associated with simple backache, neck and shoulder strains

Warnings

For external use onlyDo not use on• wounds or damaged skinWhen using this product• avoid contact with eyes or mucous membranes• do not bandage tightly or use with a heating padStop use and ask a doctor if• condition worsens• symptoms persist for more than 7 days• symptoms clear up and occur again within a few days• excessive skin irritation developsIf pregnant or breast-feedingask a health professional before useKeep out of reach of childrenIf swallowed, get medical help or contact a Poison Control Center immediately

Directions

Adults and children 12 years of age and older:• apply to affected area not more than 3 to 4 times daily.• wash hands with soap and water after use (unless applying to hands).Children under 12 years of age: ask a doctor

Inactive Ingredients

Cottonseed oil, beeswax, CBD hemp oil, clove oil, eucalyptus oil, jojoba seed oil, peppermint oil, tea tree oil, sorbic acid

Questions?

Call 1-844-422-3633

* Please review the disclaimer below.