NDC 71020-002 Antibacterial

NDC Product Code 71020-002

NDC CODE: 71020-002

Proprietary Name: Antibacterial 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.

NDC Code Structure

  • 71020 - Sante Manufacturing Inc

NDC 71020-002-16

Package Description: 500 mL 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

Antibacterial with NDC 71020-002 is a product labeled by Sante Manufacturing Inc. 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: 1046593.

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.

  • DITETRACYCLINE TETRASODIUM EDETATE (UNII: WX0A0IT7K5)
  • FD&C RED NO. 4 (UNII: X3W0AM1JLX)
  • WATER (UNII: 059QF0KO0R)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • SODIUM LAURETH SULFATE (UNII: BPV390UAP0)

Product Labeler Information

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

Labeler Name: Sante Manufacturing Inc
Labeler Code: 71020
Start Marketing Date: 10-08-2016 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.

Antibacterial 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

Benzalkonium Chloride - 0.13%

Otc - Purpose

Purpose - Antibacterial

Indications & Usage

Uses for handwashing or decrease bacteria to the skin

Otc - Stop Use

Stop use and ask a doctor If irritation or redness develops

Warnings

Warning for external use only

Otc - When Using

  • When using this productdo not get into eyes. If contact occurs, rinse eyes thoroughly with water

Otc - Keep Out Of Reach Of Children

Keep out of reach of childrenIf swallowed get medical help or contact a Poison Control Center right away

Dosage & Administration

  • DirectionWet handsapply palmful to handsscrub thoroughlyrinse

Inactive Ingredient

Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Citric Acid, Glycerin, Tetrasodium EDTA, Methylcholoroisothiazolinone, Methylisothiazolinone, Yellow #5 (Cl 19140), Red #4 (Cl 14700)

* Please review the disclaimer below.