NDC 72744-778 Cool Breeze

Menthol, Methyl Salicylate

NDC Product Code 72744-778

NDC 72744-778-40

Package Description: 113 g in 1 TUBE

NDC Product Information

Cool Breeze with NDC 72744-778 is a a human over the counter drug product labeled by Cool Breeze Us Llc. The generic name of Cool Breeze is menthol, methyl salicylate. The product's dosage form is gel and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 2105836.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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.

Cool Breeze 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.

  • WATER (UNII: 059QF0KO0R)

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: Cool Breeze Us Llc
Labeler Code: 72744
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: 12-06-2021 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.

Cool Breeze Product Label Images

Cool Breeze 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

Menthol  5.0%Methyl Salicylate  4.0%


External analgesic


Temporarily relieves minor pain associated with:• Arthritis | Backache | Muscles | Strains | Sprains | Bruises | Cramps


• Flammable keep away from fire or flame• For external use only• Store in cool dry placeWhen using this product - use only as directed• Do not bandage tightly or use with a heating pad• Avoid contact with eyes and mucus membranes• Do not apply to wounds or damaged, broken or irritated skin• A burning sensation may occur upon application but generally disappearsIf gel comes in contact with eyes, wash with warm waterStop use and ask a doctor if• Condition worsens• Symptoms persists for more than 7 days or pain continues to occurIf pregnant or breast-feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children, In case of accidental ingestion, Get medical help or contact a Poison Control Center right away.


Adults and children over 12 years:• Apply generously to affected area.• Massage into painful area until thoroughly absorbed into skin• Repeat as necessary, But no more than 4 times dailyChildren 12 years or younger:• Please speak with a doctor

Inactive Ingredients:

A non-alkaline base with water and color.

* Please review the disclaimer below.