NDC 75029-060 Heina 70% Isopropyl Alcohol

70% Isopropyl Alcohol

NDC Product Code 75029-060

NDC 75029-060-05

Package Description: 237 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Heina 70% Isopropyl Alcohol with NDC 75029-060 is a a human over the counter drug product labeled by Corechem Inc.. The generic name of Heina 70% Isopropyl Alcohol is 70% isopropyl alcohol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Corechem Inc.

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.

Heina 70% Isopropyl 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.
  • 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: Corechem Inc.
Labeler Code: 75029
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: 10-26-2020 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.

Heina 70% Isopropyl 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

Otc Active Ingredient

Active IngredientEthyl alcohol 70% v/v

Otc Purpose Section

PurposeFirst Aid Antiseptic

Indications & Usage Section

Use First aid to help prevent the risk of infection in minor cuts, scrapes, and burns.

Warnings Section


For external use only. • if taken internally, serious gastric disturbances will result.
Flammable, keep away from fire or flame.

• use only in well-ventilated area; fumes may be toxic.

Otc Ask A Doctor

Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns.

Otc When Using Section

When using this product • do not get in eyes • do not apply over large areas of the body • do not use longer than one week unless directed by a doctor

Otc Stop Use Section

Stop use and ask a doctor if condition persists or gets worse.

Otc Keep Out Of Reach Of Children Section

Keep out of reach of children.

In case of ingestion, get medical help or contact a Poison Control Center right away.

Dosage & Administration Section

Directions • clean affected area • apply small amount of this product on the area 1-3 times daily

• if bandaged, let dry first

• may be covered with a sterile bandage

Storage & Handling Section

Other information • store at room temperature • does not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive Ingredients Section

Inactive ingredient Purified water

Full Package Label

HEINA Healthy Lifestyle70% Isopropyl AlcoholFirst Aid AntisepticHelps prevent the risk of infection in minor cuts, scrapes and burnsWARNING


8 FL OZNDC 75029-060-05www.ubbrands,comUB BrandsFor a Healthy LifestyleDist. By UB BRANDS INC

Atlanta, GA 30326

Made in USA
BARCODE7 50258 36270 1

* Please review the disclaimer below.