NDC 70677-0056 Ethyl Rubbing Alcohol
Ethyl Alcohol Liquid Topical

Product Information

Ethyl Rubbing Alcohol is a human over the counter drug product labeled by Strategic Sourcing Services Llc. The generic name of Ethyl Rubbing Alcohol is ethyl alcohol. The product's dosage form is liquid and is administered via topical form.

Product Code70677-0056
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Ethyl Rubbing Alcohol
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Ethyl Alcohol
Product Type 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.
Human Otc Drug
Dosage FormLiquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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.
Strategic Sourcing Services Llc
Labeler Code70677
FDA Application Number 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.
part333A
Marketing Category 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.
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
05-18-2009
Listing Expiration Date 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.
12-31-2023
Exclude Flag 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".
N
NDC Code Structure

What are the uses for Ethyl Rubbing Alcohol?


Product Packages

NDC 70677-0056-1

Package Description: 473 mL in 1 BOTTLE, PLASTIC

Product Details

What are Ethyl Rubbing Alcohol Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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.
  • ACETONE (UNII: 1364PS73AF)
  • DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
  • METHYL ISOBUTYL KETONE (UNII: U5T7B88CNP)
  • WATER (UNII: 059QF0KO0R)

* Please review the disclaimer below.

Ethyl Rubbing Alcohol Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Active Ingredient



Ethyl alcohol 70%


Purpose



First aid antiseptic


Use



first aid to help prevent the risk of infection in:

  • minor cuts
  • scrapes
  • burns

Warnings



For external use only.

Flammable. Keep away from fire or flame, heat, spark, electrical


Ask A Doctor Before Use



for deep or puncture wounds, animal bites or serious burns


When Using This Product



  • do not get into eyes
  • do not inhale
  • do not apply over large areas of the body
  • do not use longer than 1 week

Stop Use And Ask A Doctor If



condition persists or gets worse


Keep Out Of Reach Of Children



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


Caution



Fumes can be acutely irritating to skin, eyes and the respiratory system.  Do not apply to irritated skin or if excessive irritation develops.  Avoid getting into the eyes or on mucous membranes.  Avoid inhaling this product.


Directions



  • clean the affected area
  • apply a small amount of this product on the affected area 1 to 3 times daily
  • may be covered with a sterile bandage
  • if bandage, let dry first

Other Information



will produce serious gastric disturbances if taken internally


Inactive Ingredient



acetone, denatonium benzoate, methyl isobutyl ketone, water


Other



McKesson

Another Quality Product Distributed by McKesson

One Post Street, San Francisco, CA 94104

Money Back Guarantee

Please visit us at www.sunmarkbrand.com

DSP-TN-15000

DSP-MO-34

SDS-TN-15012

Pat. D675,101


Principal Display Panel



Sunmark

Ethyl rubbing alcohol 70% by volume

First Aid Antseptic

For rubbing and massaging

For treatment of minor cuts and scrapes

WARNING FLAMMABLE Keep away from heat, spark, electrical, fire or flame

Use only in well-ventilated area; fumes can be harmful

CAUTION: Do not point at self or others; product will squirt when squeezed.

16 FL OZ (1 PT) 473 mL


* Please review the disclaimer below.