Xerac Ac
Person And Covey
Human Otc Drug
NDC 0096-0709Xerac Ac is a human otc drug labeled by 'Person And Covey'. National Drug Code (NDC) number for Xerac Ac is 0096-0709. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Xerac Ac drug includes Aluminum Chloride - .0625 g/g . The currest status of Xerac Ac drug is Active.
Drug Information:
| Drug NDC: | 0096-0709 |
| 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: | Xerac Ac |
| 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: | Xerac Ac |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Person And Covey |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Liquid |
| 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 CHLORIDE - .0625 g/g
|
| 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: | 01 Jun, 1996 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 14 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: | part350 |
| 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, 2023 |
| 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: | Person and Covey
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 197324
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | 3CYT62D3GA
|
| 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 |
|---|
| 0096-0709-35 | 29.09 g in 1 PACKAGE (0096-0709-35) | 01 Jun, 1996 | N/A | No |
| 0096-0709-60 | 49.86 g in 1 PACKAGE (0096-0709-60) | 01 Jun, 1996 | 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:
Otc - purpose section for topical application as an antiperspirant (anhidrotic).
Product Elements:
Xerac ac xerac ac alcohol aluminum chloride aluminum cation
Indications and Usage:
Indicatins and usage section for patients suffering from hyperhidrosis, or patients whose jobs or sports activities cause excessive sweating that exacerbates other skin problems.
Warnings:
Warnings section for external use only. avoid contact with eyes. if contact occurs, wash eyes thoroughly with water. if irritation or sensitization occurs, discontinue use or contact a physician. xerac ac may be harmful to cotton fibers and certain metals.
Dosage and Administration:
Dosage & administration section xerac ac when applied to the underarms, should be applied to absolutely dry skin. only apply xerac ac before bedtime, since medication should be kept on the skin for 6-8 hours. to reduce irritation, let the alcohol evaporate, leaving a thin film of antiperspirant on the skin. wear a t-shirt, while sleeping to prevent medication from being rubbed off on the bed linens. do not apply xerac ac to broken, irritated or recently shaved skin. wash the treated area next morning with soap and water. do not apply other deodorants or antiperspirants while using xerac ac.
Package Label Principal Display Panel:
Principal display panel xerac ac 35cc xerac ac 60cc