NDC 44224-2410 The Itch Eraser Max Strength

NDC Product Code 44224-2410

NDC 44224-2410-0

Package Description: 1 BOTTLE, SPRAY in 1 BOX > 28 mL in 1 BOTTLE, SPRAY

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

The Itch Eraser Max Strength with NDC 44224-2410 is a product labeled by Tender Corporation. The generic name of The Itch Eraser Max Strength is . The product's dosage form is and is administered via form.

Labeler Name: Tender Corporation

Dosage Form: -

Product Type: 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.

  • WATER (UNII: 059QF0KO0R)
  • POVIDONES (UNII: FZ989GH94E)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SODIUM BICARBONATE (UNII: 8MDF5V39QO)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • TEA TREE OIL (UNII: VIF565UC2G)
  • ZINC ACETATE (UNII: FM5526K07A)

Product Labeler Information

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

Labeler Name: Tender Corporation
Labeler Code: 44224
Start Marketing Date: 12-04-2015 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: 12-31-2019 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: I 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.

Information for Patients

Diphenhydramine

Diphenhydramine is pronounced as (dye fen hye' dra meen)

Why is diphenhydramine medication prescribed?
Diphenhydramine is used to relieve red, irritated, itchy, watery eyes; sneezing; and runny nose caused by hay fever, allergies, or the common cold. Diphenhydramine is als...
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Diphenhydramine Topical

Diphenhydramine Topical is pronounced as (dye fen hye' dra meen)
Why is diphenhydramine topical medication prescribed?
Diphenhydramine, an antihistamine, is used to relieve the itching of insect bites, sunburns, bee stings, poison ivy, poison oak, and minor skin irritation.This medication...
[Read More]

* Please review the disclaimer below.

The Itch Eraser Max Strength Product Label Images

The Itch Eraser Max Strength 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 Ingredients:

Diphenhydramine HCl 2%

​Purpose:

Topical analgesic

​Uses

​For temporary relief of pain and itching associated with:​



• insect bites • minor burns • sunburn • minor skin irritations • minor cuts • scrapes • rashes due to poison: ivy, oak and sumac

​Warnings

​For external use only​



• do not get into eyes​




Stop Use And Ask A Doctor If

• condition worsens • symptoms last 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.

Do Not Use

• on large areas of tyhe body • with any other product containing diphenhydramine, even one taken by mouth

Ask A Doctor Before Use

• on chicken pox • on measles

​Directions

  • ​do not use more often than directedadults and children 2 years of age and older: ​apply to affected area not more than 3 to 4 times daily.
  • Children under 2 years of age​: ask a doctor.

​Inactive Ingredients

SD Alcohol 40-2, Purified Water, Povidone, Glycerin, Oat Beta Glucan, Sodium Bicarbonate (Baking Soda), Vitamin E Acetate, Tea Tree Oil, and Zinc Acetate

* Please review the disclaimer below.