Canna Numb Roll On Liquid
FDA Label NDC 72614-265

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cannanumb Llc for the product Canna Numb Roll On (NDC 72614-265). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients, purpose, uses:, warnings:, do not use, when using this product, stop use and ask a doctor if, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Lidocaine HCl 4%

Menthol 1%

Purpose

Topical Anesthetic

Topical Analgesic

Uses:

  • temporarily relieves minor pain

Warnings:

For external use only.

Do Not Use

  • on large areas of the body or on cut, irritated or swollen skin 
  • on puncture wounds
  • for more than one week without consulting a doctor

When Using This Product

  • use only as directed. Read and follow directions and warnings on this package.
  • Avoid contact with eyes and mucous membranes
  • rare cases of serious burns have been reported with products of this type 
  • do not apply to wounds or damaged, broken or irritated skin 
  • do not bandage tightly or apply local heat (such as heating pads) or a medicated patch to the area of use
  • a transient burning sensation may occur upon application but generally disappears in several days
  • avoid applying into skin folds

Stop Use And Ask A Doctor If

  • conditions worsens
  • redeness is present
  • irritation develops 
  • symptoms persist for more than 7 days or clear up and occur again within a few days
  • you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied
  • Flammable - keep away from fire or flame

If Pregnant Or Breast-Feeding,

ask a health professional before use.

Keep Out Of Reach Of Children And Pets.

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

Directions:

adults and children over 12 years:

  • apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period
  • massage into painful area until thoroughly absorbed into skin 
  • children 12 years or younger: ask a doctor

Inactive Ingredients:

Aqua (Deionized Water), Arnica Montana Extract, Boswellia Serrata Extract, Cannabis Sativa (Hemp) Seed Oil, Carbomer, Citrus Aurantium Dulcis (Orange) Oil, Ethylhexylglycerin, Glucosamine Sulfate, Ilex Paraguayensis (Yerba Mate) Extract, Magnesium Sulfate, Methylsulfonylemthane (MSM), Phenoxyethanol, Polysorbate-20, Propylene Glycol, Salix Nigra (Willow) Bark Extract, Sd-Alcohol 40B, Triethanolamine.

Package Labeling:

Label4 (Label4)

Label4 (Label4)

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