NDC 73306-1108 Antiperspirant Above Teen Be Positive

Antiperspirant Above Teen Be Positive Aerosol

NDC Product Code 73306-1108

NDC Code: 73306-1108

Proprietary Name: Antiperspirant Above Teen Be Positive 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.

Non-Proprietary Name: Antiperspirant Above Teen Be Positive Aerosol What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 73306 - Baston Industria De Aeross�is Ltda
    • 73306-1108 - Antiperspirant Above Teen Be Positive

NDC 73306-1108-1

Package Description: 90 g in 1 CAN

NDC Product Information

Antiperspirant Above Teen Be Positive with NDC 73306-1108 is a a human over the counter drug product labeled by Baston Industria De Aeross�is Ltda. The generic name of Antiperspirant Above Teen Be Positive is antiperspirant above teen be positive aerosol. The product's dosage form is aerosol, spray and is administered via topical form.

Labeler Name: Baston Industria De Aeross�is Ltda

Dosage Form: Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous solvents.

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.

Antiperspirant Above Teen Be Positive 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 SESQUICHLOROHYDRATE 24 g/100g

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.

  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • MACADAMIA OIL (UNII: 515610SU8C)
  • POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
  • COCONUT (UNII: 3RT3536DHY)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • LEVANT COTTON SEED (UNII: 550E4N439V)
  • SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)
  • ALLANTOIN (UNII: 344S277G0Z)
  • CHAMOMILE (UNII: FGL3685T2X)
  • PROPANE (UNII: T75W9911L6)
  • ARGAN OIL (UNII: 4V59G5UW9X)
  • VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
  • MYRRH OIL (UNII: H74221J5J4)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • BUTANE (UNII: 6LV4FOR43R)
  • ISOBUTANE (UNII: BXR49TP611)
  • LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
  • DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
  • WATER (UNII: 059QF0KO0R)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • AVOCADO OIL (UNII: 6VNO72PFC1)
  • GREEN TEA LEAF (UNII: W2ZU1RY8B0)
  • CINNAMON BARK OIL (UNII: XE54U569EC)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • SHEA BUTTER (UNII: K49155WL9Y)
  • PROPYLENE CARBONATE (UNII: 8D08K3S51E)

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.

Product Labeler Information

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

Labeler Name: Baston Industria De Aeross�is Ltda
Labeler Code: 73306
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: 09-11-2019 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: 12-31-2020 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’.

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