NDC 80955-010 Purity Bleu Antibacterial

Product Information

Purity Bleu Antibacterial is product labeled by Alben Internacional, S.a. De C.v.. The product's dosage form is and is administered via form.

Product Code80955-010
Proprietary Name 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.
Purity Bleu Antibacterial
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Alben Internacional, S.a. De C.v.
Labeler Code80955
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
03-30-2020
Listing Expiration Date 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.
12-31-2021
Exclude Flag 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".
I
NDC Code Structure

What are the uses for Purity Bleu Antibacterial?


Product Packages

NDC 80955-010-01

Package Description: 250 mL in 1 BOTTLE, PUMP

NDC 80955-010-02

Package Description: 1000 mL in 1 BOTTLE, DISPENSING

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

Product Details

What are Purity Bleu Antibacterial Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
  • BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
  • BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)

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.
  • ALOE (UNII: V5VD430YW9)
  • BENZOPHENONE-5 (UNII: 853Z42ZYAS)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • COCO DIETHANOLAMIDE (UNII: 92005F972D)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)
  • SODIUM LAURYL SULFATE (UNII: 368GB5141J)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • WATER (UNII: 059QF0KO0R)

* Please review the disclaimer below.

Purity Bleu Antibacterial Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Otc - When Using



When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


Otc - Stop Use



Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.


Otc - Keep Out Of Reach Of Children



Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


* Please review the disclaimer below.