NDC 42265-101 Unblem Est

NDC Product Code 42265-101

NDC 42265-101-12

Package Description: 28 g in 1 BOTTLE, PLASTIC

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

NDC Product Information

Unblem Est with NDC 42265-101 is a product labeled by Elli Est. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 106315.

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)
  • POLYACRYLAMIDE (CROSSLINKED; 0.01-0.2 MOLE PERCENT BISACRYLAMIDE) (UNII: RHA9LWJ494)
  • C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
  • LAURETH-7 (UNII: Z95S6G8201)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)

Product Labeler Information

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

Labeler Name: Elli Est
Labeler Code: 42265
Start Marketing Date: 10-25-2012 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: 12-31-2017 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 - INACTIVATED, the listing data was inactivated by the FDA. 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Information for Patients

Benzoyl Peroxide Topical

Benzoyl Peroxide Topical is pronounced as (ben' zoe il)

Why is benzoyl peroxide topical medication prescribed?
Benzoyl peroxide is used to treat mild to moderate acne....
[Read More]

* Please review the disclaimer below.

Unblem Est Product Label Images

Unblem Est 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 Ingredients: Benzoyl Peroxide 10%

Otc - Purpose

Purpose: Acne Treatment

Otc - Keep Out Of Reach Of Children

Keep out of reach of children: ifswallowed, get medical help or contact a poison control center right away

Indications & Usage

Usage: For external use only.Do not use if: you have very sensitiveskin are sensitive to benzoyl peroxide.

Warnings

Warning: For external use only.Do not use if you- have very sensitive skin-are sensitive to benzoyl peroxide.Keep 0ut of reach of children. If swallowed, get medical help or contact a poison control center right away.When using this product -keep away from eyes, lips and mouth.- If contact occurs, flush thoroughly with water.- If going outside apply sunscreen after using this product.-If irritation or sensitivity develops, stop use of both products and ask a doctor.Avoid contact with hair or dyed fabric,including carpet and clothing which may be bleached by this product.-skin irritation may occur ,characterized by redness, burning , itching, peeling or possibly swelling.Mild irritation may be reduced by using the product less frequently or in a lower concentration. -If irritation becomes sever, discontinue use.If irritation still continues ,consult a doctor.-Using other topical acne medication at the same time or immediately following the use of this product may increase dryness or irritation of the skin.If this occurs only one medication should be used unless directed by a doctor

Dosage & Administration

Directions: Cleanse the skin thoroughly before applying medication.- Cover the entire affected area with a thin layer 1 to 3 times daily. -If bothersome dryness or peeling occurs, reduce application to once a day or every other day.- Because of excessive drying of the skin may occur start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.

Inactive Ingredient

Inactive Ingredients: Water (Aqua), Polyacrylamide crosslinked 0.01-0.2 mole percent bisacrlyamidC-13-14 Isoparafin, laureth-7, Methylparaben, Propylparaben.

* Please review the disclaimer below.