NDC 81547-001 Colemerg 75 Alcohol Sanitizing


NDC Product Code 81547-001

NDC 81547-001-01

Package Description: 547 mL in 1 CAN

NDC Product Information

Colemerg 75 Alcohol Sanitizing with NDC 81547-001 is a a human over the counter drug product labeled by Ksmt Company Incorporated. The generic name of Colemerg 75 Alcohol Sanitizing is alcohol. The product's dosage form is spray and is administered via topical form.

Labeler Name: Ksmt Company Incorporated

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Colemerg 75 Alcohol Sanitizing 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.

  • ALCOHOL 75 mL/100mL

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.

  • PROPANE (UNII: T75W9911L6)

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: Ksmt Company Incorporated
Labeler Code: 81547
FDA Application Number: part333E 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: 10-25-2020 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.

Colemerg 75 Alcohol Sanitizing Product Label Images

Colemerg 75 Alcohol Sanitizing 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 Ingredient

Ethyl Alcohol 75%




  • Decreases bacteria on the skinRecommended for repeated use


  • Extermely flammable aerosol, keep away from fire / flame.Keep away from heat, hot surfaces, open flames and other ignition sources.Pressurized contiainer, Do not pierce or burn, even after use.Protect from the sunlight.For external use only

Do Not Use

  • On children less than 2 months of ageOn open skin wounds

When Using This Product

  • Avoid use on/or around eyes, ears, mouth, broken/irritated skin or large areas of body.In case of contact with eyes, rinse thoroughly with water for several minutes.Do not inhale or ingest

Stop And Ask A Doctor If

  • Irritation persistIf product is swallowed

Keep Out Of Reach Of Children.

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


  • Shake well before use.Hold can upright at 6-7 inches away from surfaces and spray evenly.Allow to air dry for 5 to 10 minutes. Repeat application as necessary.Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

  • Store between 15-30° C (59-86°F)Do not expose to temperature exceeding 50 C/122 F.

Inactive Ingredients

Butane, Fragrance, Isobutane, Propane.

* Please review the disclaimer below.