NDC 78056-099 Tsc 99% Isopropyl Alcohol

Isopropyl Alcohol

NDC Product Code 78056-099

NDC 78056-099-01

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

NDC 78056-099-08

Package Description: 236 mL in 1 BOTTLE, SPRAY

NDC Product Information

Tsc 99% Isopropyl Alcohol with NDC 78056-099 is a a human over the counter drug product labeled by Ts Cosmetic Labs, Inc.. The generic name of Tsc 99% Isopropyl Alcohol is isopropyl alcohol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Ts Cosmetic Labs, 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.

Tsc 99% 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: Ts Cosmetic Labs, Inc.
Labeler Code: 78056
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: 09-01-2020 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.

Tsc 99% 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


  • This is a Rubbing Alcohol consisting of 70% Isopropyl Alcohol.This Rubbing Alcohol is manufacture using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation):Isopropyl Alcohol (USP or meeting Criteria of USP) (99.9%, volume/volume (v/v))Purified water (0.1% v/v)This firm does not add other active or inactive ingredients than those stated above.

Active Ingredient (By Volume)

Alcohol 99% v/v. Purpose: First Aid Antiseptic


First Aid Antiseptic


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


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

Ask A Doctor Before Use If You Have

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

When Using This Product

  • When using this productdo not get into eyesdo not apply over large areas of the bodydo not use longer than one week unless directed by a doctor

Stop Use And Ask A Doctor

  • Stop use and ask a doctorcondition persists or gets worse.

Keep Out Of Reach Of Children

Keep out of reach of children. If case of ingestion, get medical help or contact a Poison Control Center immediately.


  • 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.

Other Information

  • Other InformationStore at room temperature.Does not contain, nor is intended as a substitute for grain or ethyl alcohol.If taken internally, serious gastric disturbances will result.

Inactive Ingredient

Purified water

* Please review the disclaimer below.