NDC 13537-138 Esika Its You Live Roll-on

NDC Product Code 13537-138

NDC CODE: 13537-138

Proprietary Name: Esika Its You Live Roll-on 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

  • 13537 - Ventura Corporation Ltd.

NDC 13537-138-01

Package Description: 50 mL in 1 BOTTLE

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

NDC Product Information

Esika Its You Live Roll-on with NDC 13537-138 is a product labeled by Ventura Corporation Ltd.. The product's dosage form is and is administered via form.

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)
  • STEARETH-2 (UNII: V56DFE46J5)
  • STEARETH-21 (UNII: 53J3F32P58)
  • DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • TRICLOSAN (UNII: 4NM5039Y5X)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • LEVOMENOL (UNII: 24WE03BX2T)
  • MAGNESIUM NITRATE (UNII: 77CBG3UN78)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Product Labeler Information

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

Labeler Name: Ventura Corporation Ltd.
Labeler Code: 13537
Start Marketing Date: 12-13-2011 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.

Esika Its You Live Roll-on Product Label Images

Esika Its You Live Roll-on 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

Other

Drug Facts

PR: Distributed by Ventura Corporation, Ltd. San Juan, Puerto Rico 00926.

Active Ingredients

Aluminum sesquichlorohydrate (17%)

Purpose

Antiperspirant

Uses

  • Reduces underarm wetness.

Warnings

For external use only.

Otc - Do Not Use

  • Do not use on broken skin.

Otc - Stop Use

  • Stop use and ask a doctor if rash and irritation occurs.

Otc - Ask Doctor

  • Ask a doctor before use if you have kidney disease.

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.

Directions

  • Apply to underarms only.

Inactive Ingredients

Aqua (water), steareth-2, ppg-15 stearyl ether, steareth-21, fragrance, dicaprylyl carbonate, cyclopentasiloxane, triclosan, cyclohexasiloxane, benzalkonium chloride, tetrasodium edta, bisabolol, magnesium nitrate, methylchloroisothiazolinone, magnesium chloride, methylisothiazolinone.

* Please review the disclaimer below.