NDC 70735-072 Aspicare

Isopropyl Rubbing Alcohol

NDC Product Code 70735-072

NDC 70735-072-08

Package Description: 236 mL in 1 BOTTLE

NDC 70735-072-16

Package Description: 473 mL in 1 BOTTLE

NDC 70735-072-28

Package Description: 3785 mL in 1 BOTTLE

NDC 70735-072-32

Package Description: 946 mL in 1 BOTTLE

NDC Product Information

Aspicare with NDC 70735-072 is a a human over the counter drug product labeled by American Private Label Products. The generic name of Aspicare is isopropyl rubbing alcohol. The product's dosage form is solution and is administered via topical form.

Labeler Name: American Private Label Products

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.

Aspicare 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: American Private Label Products
Labeler Code: 70735
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: 03-08-2021 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.

Aspicare Product Label Images

Aspicare 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

Isopropyl Alcohol 70% v/v.


First Aid Antiseptic


  • Helps prevent the risk of infection in:minor cutsscrapesburns


For external use only.Flammable • Keep away from fire or flame, heat, spark, or electrical

Ask A Doctor Before Use

Or 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

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


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.


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


  • Store below 110°F (43°C)May discolor certain fabrics or surfaces

Inactive Ingredients

Water (Aqua)

Other Information

Does not contain, nor is intended as a substitute for grain or ethyl alcohol • will produce serious gastric disturbances if taken internally.

* Please review the disclaimer below.