NDC 77462-007 Bebak Ayak Deodorant

Antiperspirant

NDC Product Code 77462-007

NDC 77462-007-05

Package Description: 200 g in 1 BOTTLE, SPRAY

NDC Product Information

Bebak Ayak Deodorant with NDC 77462-007 is a a human over the counter drug product labeled by Sora Kozmetik Sanayi Ticaret Anonim Sirketi. The generic name of Bebak Ayak Deodorant is antiperspirant. The product's dosage form is spray and is administered via topical form.

Labeler Name: Sora Kozmetik Sanayi Ticaret Anonim Sirketi

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Bebak Ayak Deodorant Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ALUMINUM CHLOROHYDRATE 3.78 g/200g

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.

  • ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CITRAL (UNII: T7EU0O9VPP)
  • PROPANE (UNII: T75W9911L6)
  • BUTANE (UNII: 6LV4FOR43R)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • ISOBUTANE (UNII: BXR49TP611)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • LIMONENE, (+)- (UNII: GFD7C86Q1W)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Sora Kozmetik Sanayi Ticaret Anonim Sirketi
Labeler Code: 77462
FDA Application Number: part350 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 07-16-2020 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: 12-31-2021 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: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Bebak Ayak Deodorant 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

Active Ingredient

Aluminum Chlorohydate...1.89%

Purpose

Antiperspirant

Uses

Prevent foot perspiration and odors caused by sweat.

Warnings

For External Use only.Keep product from heat, hot surfaces, sparks, flames and their ignition sources. Do not smoke when using the product. Do not expose to sunilight and temperature above 50 degrees C. The product is in a pressurized container. Do not puncture or burn the empty container; it might explode when heated. Do not inhale spray.

Otc - When Using

Avoid Contract eith eyes. Immediately wash with plenty of water in case of contact with the eyes.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Directions

Keep container 20cm away and spary on your clean and dtry feet. You may also spray into your shoes to achieve better results.

Inactive Ingredients

Butane, Isobutane, Propane, Cyclopentasiloxane, Alcohol denat., Isopropyl Alcohol, Aluminum starch octenylsuccinate, parfum, glycerin, citral, d-limonene

* Please review the disclaimer below.