NDC 70082-222 Isopropyl Rubbing Alcohol
Isopropyl Alcohol
NDC Product Code 70082-222
Proprietary Name: Isopropyl Rubbing Alcohol 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.
Non-Proprietary Name: Isopropyl Alcohol 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.
NDC Code Structure
- 70082 - Dealmed Medical Supplies Llc
- 70082-222 - Isopropyl Rubbing Alcohol
NDC 70082-222-16
Package Description: 473 mL in 1 BOTTLE, PLASTIC
NDC Product Information
Isopropyl Rubbing Alcohol with NDC 70082-222 is a a human over the counter drug product labeled by Dealmed Medical Supplies Llc. The generic name of Isopropyl Rubbing Alcohol is isopropyl alcohol. The product's dosage form is solution and is administered via topical form.
Labeler Name: Dealmed Medical Supplies Llc
Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
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.
Isopropyl Rubbing Alcohol 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: Dealmed Medical Supplies Llc
Labeler Code: 70082
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: 07-18-2018 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.
Isopropyl Rubbing Alcohol Product Label Images
Isopropyl Rubbing Alcohol 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
- Other
- Active Ingredient
- Purpose
- Uses
- Warnings
- Otc - Ask Doctor
- Otc - When Using
- Otc - Stop Use
- Otc - Keep Out Of Reach Of Children
- Directions
- Other Information
- Inactive Ingredient
Other
Drug Facts
Active Ingredient
Isopropyl Alcohol 70%
Purpose
First Aid Antiseptic
Uses
First aid to help prevent the risk of infection in: minor cuts, scrapes, burns
Warnings
For external use onlyFlammableKeep away from fire or flame, heat, spark, electricalDo not use with electrocautery procedures
Otc - Ask Doctor
Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns
Otc - When Using
When using this productdo not get into eyesdo ot apply over large areas of the bodydo not use longer than 1 week unless directed by a doctor
Otc - Stop Use
Stop use and ask a doctor if condition persists or gets worse
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
Directions
Clean the affected areaApply a small amount of this product 1 to 3 times dailyMay be covered with a sterile bandageIf bandaged, let dry first
Other Information
Does not contain, nor is intended as a substitute for grain or ethyl alcoholWill produce serious gastric disturbances if taken internally
Inactive Ingredient
Purified water
* Please review the disclaimer below.