NDC 52410-1041 Wise Shopper 50% Isopropyl Rubbing Alcohol W/ Wintergreen

Isopropyl Alcohol

NDC Product Code 52410-1041

NDC CODE: 52410-1041

Proprietary Name: Wise Shopper 50% Isopropyl Rubbing Alcohol W/ Wintergreen 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

  • 52410 - Shield Line Llc

NDC 52410-1041-4

Package Description: 355 mL in 1 BOTTLE

NDC 52410-1041-6

Package Description: 475 mL in 1 BOTTLE

NDC Product Information

Wise Shopper 50% Isopropyl Rubbing Alcohol W/ Wintergreen with NDC 52410-1041 is a a human over the counter drug product labeled by Shield Line Llc. The generic name of Wise Shopper 50% Isopropyl Rubbing Alcohol W/ Wintergreen is isopropyl alcohol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Shield Line Llc

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.

Wise Shopper 50% Isopropyl Rubbing Alcohol W/ Wintergreen 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.

  • ISOPROPYL ALCOHOL 50 mL/100mL

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.

  • METHYL SALICYLATE (UNII: LAV5U5022Y)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • 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: Shield Line Llc
Labeler Code: 52410
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: 01-01-2020 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: 12-31-2020 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.

Wise Shopper 50% Isopropyl Rubbing Alcohol W/ Wintergreen Product Label Images

Wise Shopper 50% Isopropyl Rubbing Alcohol W/ Wintergreen 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

Drug Facts

Isopropyl Alcohol (50% v/v)

Purpose

First Aid Antiseptic

Uses

  • First aid to help prevent the risk of infection inminor cutsscrapesburns

Warnings For External Use Only

  • Flammable, keep away from fire and flame
  • If taken internally, serious gastric disturbances will result

Ask A Doctor Before Use If You Have

  • Deep or puncture wounds, animal bites or serious burns

When Using This Product

  • Do not get into eyesdo not apply over large areas of the bodydo not use longer than one week unless directed by a doctordo not use otherwise than directed

Stop Use And Ask A Doctor If

  • Condition persists or gets worse

Keep Out Of Reach Of Children

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

Dosage & Administration

  • Clean the affected areaapply a small amount of this product on area 1 to 3 times dailyif bandaged, let dry firstmay be covered with sterile bandage

Other Information

  • Store at room temperaturedoes not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive Ingredients

FD&C Blue No.1, FD&C Yellow No. 5, Methyl Salicylate, Water

* Please review the disclaimer below.