NDC 69842-414 Cvs Health Sports Kit

Isopropyl Alcohol, Bacitracin Zinc,neomycin Sulfate,polymyxin B Sulfate

NDC Product Code 69842-414

NDC Code: 69842-414

Proprietary Name: Cvs Health Sports Kit 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, Bacitracin Zinc,neomycin Sulfate,polymyxin B Sulfate 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

  • 69842 - Cvs Pharmacy Inc

NDC 69842-414-01

Package Description: 1 KIT in 1 KIT * .9 g in 1 TUBE (44224-0013-4) * .5 mL in 1 POUCH (44224-0010-0)

NDC Product Information

Cvs Health Sports Kit with NDC 69842-414 is a a human over the counter drug product labeled by Cvs Pharmacy Inc. The generic name of Cvs Health Sports Kit is isopropyl alcohol, bacitracin zinc,neomycin sulfate,polymyxin b sulfate. The product's dosage form is kit and is administered via form.

Labeler Name: Cvs Pharmacy Inc

Dosage Form: Kit - A packaged collection of related material.

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.

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.

  • PETROLATUM (UNII: 4T6H12BN9U)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Cvs Pharmacy Inc
Labeler Code: 69842
Marketing Category: UNAPPROVED DRUG OTHER - 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: 09-01-2019 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: 12-31-2020 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.

Cvs Health Sports Kit 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

Purpose

Antiseptic

First Aid Antibiotic

Use

For preparation of skin before injection.

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

Warnings

For external use only.Flammable - keep away from fire or flame

For external use only.

Do Not Use

  • In the eyeswith electrocautery procedures

  • If you are allergic to any of the ingredientsin the eyesover large areas of the body

Stop Use And Ask A Doctor If

  • Irritation and redness developcondition persists for more than 72 hours

Symptoms persist for more than 7 days or clear up and occur again within a few days.

Keep Out Of Reach Of Children

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

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

Directions

Wipe Injection site vigorously and discard.

  • Adults and children 2 year of age and older: clean the affected area; apply a small amount to the area 1-3 times daily; may be covered with a sterile bandagechildren under 2 years of age: consult a doctor

Other Information

Store at room temperature 15-30 degree Celsius (59-86 degree Fahrenheit)

Inactive Ingredient

Purified water

Active Ingredients

Bacitracin Zinc 400 unitsNeomycin Sulfate 5mg ( equivalent to 3.5 mg Neomycin base)Polymyxin B Sulfate 5000 units

Ask A Doctor Before Use If You Have

  • Deep pumcture woundsanimal bitesserious burns

Inactive Ingredients

Mineral oil, petrolatum

* Please review the disclaimer below.