V-activ For Men
Capsicum Frutescens, Capsicum Annuum
Hot Productions And Vertriebs Gmbh
Human Otc Drug
NDC 71326-204V-activ For Men also known as Capsicum Frutescens, Capsicum Annuum is a human otc drug labeled by 'Hot Productions And Vertriebs Gmbh'. National Drug Code (NDC) number for V-activ For Men is 71326-204. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in V-activ For Men drug includes Capsicum Annuum Whole - .1 g/100mL Capsicum Frutescens Whole - .1 g/100mL . The currest status of V-activ For Men drug is Active.
Drug Information:
| Drug NDC: | 71326-204 |
| 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: | V-activ For Men |
| 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: | Capsicum Frutescens, Capsicum Annuum |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Hot Productions And Vertriebs Gmbh |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | 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: | CAPSICUM ANNUUM WHOLE - .1 g/100mL
CAPSICUM FRUTESCENS WHOLE - .1 g/100mL
|
| 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: | UNAPPROVED HOMEOPATHIC |
| 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: | 06 Apr, 2017 |
| 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. |
| 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: | HOT PRODUCTIONS AND VERTRIEBS GMBH
|
| 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. |
| UNII: | 7FKZ3QQQ1F
6XJX33L87P
|
| 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 |
|---|
| 71326-204-51 | 1 BOTTLE, SPRAY in 1 BOX (71326-204-51) / 50 mL in 1 BOTTLE, SPRAY (71326-204-11) | 06 Apr, 2017 | 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:
Purpose topical anesthetic
Product Elements:
V-activ for men capsicum frutescens, capsicum annuum aloe vera leaf propylene glycol panthenol camphor oil cetostearyl alcohol vanillyl butyl ether capsicum annuum whole capsicum annuum whole anhydrous citric acid glycerin sunflower oil sodium benzoate potassium sorbate polidocanol water capsicum frutescens whole capsicum frutescens whole sorbitol
Indications and Usage:
Use v-activ penis power spray is a highquality treatment spray for special erotic enjoyment. apply the spray just prior to sexual intercourse for a spontaneously lust-full experience.
Warnings:
Warnings do not allow it to contact the eyes or areas of open skin. do not use during pregnancy!
Dosage and Administration:
Directions pump the v-activ penis power spray a few times to moisten the entire penis and testes area and allow it to take effect. wait approx. 2-3 minutes for the spray to be completely absorbed before putting on a condom.
Package Label Principal Display Panel:
0-uc_v activ