NDC 72197-027 Pharmacys Prescription Hand Sanitizer


NDC Product Code 72197-027

NDC 72197-027-99

Package Description: 3785.41 mL in 1 BOTTLE

NDC Product Information

Pharmacys Prescription Hand Sanitizer with NDC 72197-027 is a a human over the counter drug product labeled by American Consumer Products Corp. The generic name of Pharmacys Prescription Hand Sanitizer is alcohol. The product's dosage form is gel and is administered via topical form.

Labeler Name: American Consumer Products Corp

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.

Pharmacys Prescription Hand Sanitizer 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 71.5 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.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: American Consumer Products Corp
Labeler Code: 72197
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: 04-28-2020 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 - 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.

Pharmacys Prescription Hand Sanitizer Product Label Images

Pharmacys Prescription Hand Sanitizer 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

Active ingredients - Ethyl Alcool 71.5%


Purpose - Antiseptic


Warnings - For external use only. Do not ingest or swallow.Flammable. Keep away from fire or flame.Do not apply around eyes. Do not use in ears & mouth.

Indications & Usage

When using this product, avoid contact with eyes. In case of contact, flush eyes with water.

Stop Use

Stop use and ask a doctor if redness or irritation develps and persists for more than 72 hours.

Keep Out Of Reach Of Children

Keep out of reach of children. Do not use on children less than 2 months of age. Supervise children under 6 years of age to prevent swallowing. If swallowed, get medical help or contact a Poison Control Center right away.


Directions - Apply as needed into your palms and thoroughly spread on both hands - rub in skin until dry.

Other Information

Other information - store at 20°C (68° to 77° F).
-may discolor fabrics.

Inactive Ingredients

INACTIVE INGREDIENTS: Purified Water (Aqua), Isopropanol, Propylene Glycol, Isopropyl Myristate

Distributed By:

Distributed By:American Consumer Products CorpVernon, CA 90058

* Please review the disclaimer below.