Cannacalming Massage Oil
Carolina Cannabis Massage Oil
Carolina Cannabis Creations L.l.c
Human Otc Drug
NDC 82876-437Cannacalming Massage Oil also known as Carolina Cannabis Massage Oil is a human otc drug labeled by 'Carolina Cannabis Creations L.l.c'. National Drug Code (NDC) number for Cannacalming Massage Oil is 82876-437. This drug is available in dosage form of Oil. The names of the active, medicinal ingredients in Cannacalming Massage Oil drug includes Arnica Montana Flower Water - 2.85 g/107.48g . The currest status of Cannacalming Massage Oil drug is Active.
Drug Information:
| Drug NDC: | 82876-437 |
| 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: | Cannacalming Massage Oil |
| 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: | Carolina Cannabis Massage Oil |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Carolina Cannabis Creations L.l.c |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Oil |
| 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: | ARNICA MONTANA FLOWER WATER - 2.85 g/107.48g
|
| 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: | 24 Aug, 2022 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 19 Jun, 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: | Carolina Cannabis Creations L.L.C
|
| 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: | 0850024328181
|
| UPC stands for Universal Product Code. |
| UNII: | U7L2JP51PR
|
| 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 |
|---|
| 82876-437-34 | 107.48 g in 1 BOTTLE (82876-437-34) | 24 Aug, 2022 | 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. |
Purpose:
Purpose topical analgesic topical analgesic
Product Elements:
Cannacalming massage oil carolina cannabis massage oil rice bran oil lavender oil peppermint oil arnica montana flower water arnica montana flower water almond oil jojoba oil cannabidiol
Indications and Usage:
Uses temporary relief of aches and pains associated with arthritis, backache, muscle pains, joint pain, bruising purpose topical analgesic topical analgesic
Warnings:
Warnings for external use only.
When Using:
When using this product do not apply to wounds or irritated skin, avoid contact with eyes, if you are allergic to the listed ingredients stop use and ask doctor if condition worsens, symptoms last for more than 7 days, condition clears up but occurs again within a few days, rash or irritation occurs stop use and ask doctor if condition worsens, symptoms last for more than 7 days, condition clears up but occurs again in a few days, rash or irritation occurs
Dosage and Administration:
Directions shake well before use. adults and children 12 years and over; apply to affected area 1-4 times daily. children under 12 years; consult a doctor keep out of reach of children keep out of reach of children
Stop Use:
Stop use and ask doctor if condition worsens, symptoms last for more than 7 days, condition clears up but occurs again in a few days, rash or irritation occurs
Overdosage:
In case of overdose seek medical help or contact a poison control center right away
Package Label Principal Display Panel:
Massage oil label