Antiperspirant Above One By Passion Women
Baston Industria De Aerossois Ltda
Human Otc Drug
NDC 73306-1141Antiperspirant Above One By Passion Women is a human otc drug labeled by 'Baston Industria De Aerossois Ltda'. National Drug Code (NDC) number for Antiperspirant Above One By Passion Women is 73306-1141. This drug is available in dosage form of Aerosol, Spray. The names of the active, medicinal ingredients in Antiperspirant Above One By Passion Women drug includes Aluminum Chlorohydrate - 16 g/100g . The currest status of Antiperspirant Above One By Passion Women drug is Active.
Drug Information:
| Drug NDC: | 73306-1141 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Antiperspirant Above One By Passion Women |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Antiperspirant Above One By Passion Women |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Baston Industria De Aerossois Ltda |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Aerosol, Spray |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | ALUMINUM CHLOROHYDRATE - 16 g/100g
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | OTC MONOGRAPH FINAL |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. |
| Marketing Start Date: | 15 Feb, 2023 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 06 May, 2026 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Application Number: | M019 |
| 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. |
| Listing Expiration Date: | 31 Dec, 2024 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | BASTON INDUSTRIA DE AEROSSOIS LTDA
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UPC: | 7899674034281
|
| UPC stands for Universal Product Code. |
| UNII: | HPN8MZW13M
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 73306-1141-1 | 86 g in 1 BOTTLE, SPRAY (73306-1141-1) | 15 Feb, 2023 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Antiperspirant
Product Elements:
Antiperspirant above one by passion women antiperspirant above one by passion women isobutane aluminum chlorohydrate aluminum chlorohydrate
Indications and Usage:
Reduces underarms wetness reduces underarms wetness
Warnings:
Warnings: flammable. do not use near heat, flame or while smoking, can cause serious injury or death. keep away from face and mouth avoid breathing in avoid spraying in eyes. contents under pressure. do not puncture or incinerate. do not expose to heat, sunlight or store at temperatures above 120ºf/50ºc or in enclosed places that could overheat. do not use on broken skin. stop ude if rash or irritation occurs. get medical attention immediately ask a doctor before using if you have kidney disease. keep out of reach ok children and animals. use only as directed. intentional misuse by deliberately concentrating and inhaling the contents can be harmeful or fatal. avoid the inhalation of the product . in case of contact with eyes, rinse with plenty of water. if swallowed, do not leave the aerosol container in a vehicle. risk of leakage and explosion. container material: aluminum. batch help stop ilhalation abuse: www.inhalant.org
Warnings and Cautions:
Uses: shake the container well and apply to the underarms approximately 15cm away. protect the eyes during the application warnings: flammable. do not use near heat, flame or while smoking, can cause serious injury or death. keep away from face and mouth avoid breathing in avoid spraying in eyes. contents under pressure. do not puncture or incinerate. do not expose to heat, sunlight or store at temperatures above 120ºf/50ºc or in enclosed places that could overheat. do not use on broken skin. stop ude if rash or irritation occurs. get medical attention immediately ask a doctor before using if you have kidney disease. keep out of reach ok children and animals. use only as directed. intentional misuse by deliberately concentrating and inhaling the contents can be harmeful or fatal. avoid the inhalation of the product . in case of contact with eyes, rinse with plenty of water. if swallowed, do not leave the aerosol container in a vehicle. risk of leakage and explosion. container mat
Read more...erial: aluminum. batch help stop ilhalation abuse: www.inhalant.org shake the container well and apply to the underarms approximately 15cm away. protect the eyes during the application
Dosage and Administration:
Apply to underarms only
Apply to underarms only apply to underarms only
Package Label Principal Display Panel:
Label
Further Questions:
Email : support@myspray.group or call (305) 677-5030 email : support@myspray.group or call (305) 677-5030