NDC 13537-132 Esika Salvaje Roll-on

NDC Product Code 13537-132

NDC 13537-132-01

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 Salvaje Roll-on with NDC 13537-132 is a product labeled by Ventura Corporation Ltd.. The generic name of Esika Salvaje Roll-on is . The product's dosage form is and is administered via form.

Labeler Name: Ventura Corporation Ltd.

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)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • TRICLOSAN (UNII: 4NM5039Y5X)
  • BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • LEVOMENOL (UNII: 24WE03BX2T)

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 Salvaje Roll-on Product Label Images

Esika Salvaje 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), ppg-15 stearyl ether, steareth-2, steareth-21, fragrance, dicaprylyl carbonate, cyclopentasiloxane, cyclohexasiloxane, triclosan, benzalkonium chloride, tetrasodium edta, methylparaben, bisabolol.

* Please review the disclaimer below.