NDC 51774-008 Professional


NDC Product Code 51774-008

NDC 51774-008-02

Package Description: 60 mL in 1 BOTTLE

NDC 51774-008-04

Package Description: 120 mL in 1 BOTTLE

NDC 51774-008-05

Package Description: 125 mL in 1 BOTTLE

NDC 51774-008-12

Package Description: 360 mL in 1 BOTTLE

NDC 51774-008-16

Package Description: 480 mL in 1 BOTTLE

NDC 51774-008-28

Package Description: 3840 mL in 1 BOTTLE

NDC 51774-008-32

Package Description: 960 mL in 1 BOTTLE

NDC Product Information

Professional with NDC 51774-008 is a a human over the counter drug product labeled by Industrias Chamer S.a. De C.v.. The generic name of Professional is alcohol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Industrias Chamer S.a. De C.v.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Professional 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 70 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.

  • 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.
  • 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: Industrias Chamer S.a. De C.v.
Labeler Code: 51774
FDA Application Number: part333A 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: 08-24-2020 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: 12-31-2021 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Professional 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


Drug Facts

Active Ingredient

Ethyl Alcohol 70% V/V



Indications & Usage

  • Clean the affected area.Spray a small amount of this product on the area 1 to 3 times daily.May be covered with sterile bandage.If bandaged, let dry first.


For external use only. Flammable — Keep away from fire or flame.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Otc - Stop Use

  • Stop use and ask a doctor if irritation or redness develops and lasts more than 72 hours.

Other Information

  • Do not store above 105 ºF (40 ºC).May discolor certain wood surfaces.

Inactive Ingredients

Aqua (Water).


M-F: 8-5 CT+1 781 519-4494

* Please review the disclaimer below.