NDC 72519-104 Xceptor Cbd Pain Menthol

Methyl Salicylate

NDC Product Code 72519-104

NDC Product Information

Xceptor Cbd Pain Menthol with NDC 72519-104 is a a human over the counter drug product labeled by Xceptor Llc. The generic name of Xceptor Cbd Pain Menthol is methyl salicylate. The product's dosage form is cream and is administered via topical form.

Labeler Name: Xceptor Llc

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 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 Additional informationCallout TooltipWhat 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.


Xceptor Cbd Pain Menthol Active Ingredient(s)

Additional informationCallout TooltipWhat is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • METHYL SALICYLATE 10 g/100mL

Inactive Ingredient(s)

Additional informationCallout TooltipAbout 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.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • BENZOIC ACID (UNII: 8SKN0B0MIM)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • BETA VULGARIS (UNII: 4G174V5051)
  • CANNABIDIOL (UNII: 19GBJ60SN5)
  • COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
  • COCONUT OIL (UNII: Q9L0O73W7L)
  • COCONUT ALKANES (UNII: 1E5KJY107T)
  • BETADEX (UNII: JV039JZZ3A)
  • DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)
  • POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
  • POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
  • SHEA BUTTER (UNII: K49155WL9Y)
  • SORBIC ACID (UNII: X045WJ989B)
  • TREMELLA FUCIFORMIS WHOLE (UNII: 4938BNS0GU)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

Additional informationCallout TooltipWhat 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

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Xceptor Llc
Labeler Code: 72519
FDA Application Number: part348 Additional informationCallout TooltipWhat 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. Additional informationCallout TooltipWhat 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: 03-11-2019 Additional informationCallout TooltipWhat 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: 12-31-2020 Additional informationCallout TooltipWhat 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 Additional informationCallout TooltipWhat 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Xceptor Cbd Pain Menthol Product Label Images

Xceptor Cbd Pain Menthol 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

METHYL SALICYLATE  10%

Purpose

TOPICAL ANALGESIC

Uses

TOPICAL PAIN RELIEF FOR MINOR ACHES AND PAINS.

Warnings

FOR EXTERNAL USE ONLY.KEEP AWAY FROM EYES.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Directions

APPLY SMALL AMOUNT TO AFFECTED AREA AND RUB IN. ADD AS NEEDED.

Other Information

STORE AT 20° - 25°C (68°-77°F)

Inactive Ingredients

ALOE BARBADENSIS LEAF JUICE EXTRACT, BENZOIC ACID, BENZYL ALCOHOL, BETA VULGARIS (BEET) ROOT EXTRACT, CANNABIDIOL FROM HEMP, COCOCAPRYLATE/CAPRATE, COCOS NUCIFERA (COCONUT) OIL, COCONUT ALKANES, CYCLODEXTRIN, DISTEARDIMONIUM HECTORITE, GLYCERIN, MAGNESIUM SULFATE, POLYGLYCERYL-3 DIISOSTEARATE, POLYGLYCERYL-3 POLYRICINOLEATE, SHEA BUTTER ETHYL ESTERS, SORBIC ACID, TREMELLA FUCIFORMIS SPOROCARP EXTRACT, XANTHAN GUM, WATER

* Please review the disclaimer below.

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