Perfect Butt Booster
Anemarrhena Asphodeloides
Hot Productions And Vertriebs Gmbh
Human Otc Drug
NDC 71326-302Perfect Butt Booster also known as Anemarrhena Asphodeloides is a human otc drug labeled by 'Hot Productions And Vertriebs Gmbh'. National Drug Code (NDC) number for Perfect Butt Booster is 71326-302. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in Perfect Butt Booster drug includes Anemarrhena Asphodeloides Root - .1 g/100mL . The currest status of Perfect Butt Booster drug is Active.
Drug Information:
| Drug NDC: | 71326-302 |
| 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: | Perfect Butt Booster |
| 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: | Anemarrhena Asphodeloides |
| 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: | Cream |
| 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: | ANEMARRHENA ASPHODELOIDES ROOT - .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: | 30 Aug, 2018 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 21 Dec, 2025 |
| 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: | U0OC9BJL0I
|
| 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 |
|---|
| 71326-302-51 | 1 TUBE in 1 BOX (71326-302-51) / 100 mL in 1 TUBE (71326-302-11) | 30 Aug, 2018 | 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 derrière care
Product Elements:
Perfect butt booster anemarrhena asphodeloides water hydrogenated polybutene (1300 mw) glycerin cetearyl olivate sorbitan olivate macadamia oil benzyl alcohol chondrus crispus carrageenan xanthan gum hydrolyzed soy protein (enzymatic; 2000 mw) benzoic acid dextrose, unspecified form sorbic acid sodium hydroxide phenoxyethanol anemarrhena asphodeloides root anemarrhena asphodeloides root
Indications and Usage:
Use a cream to stimulate derrière enhancement.
Warnings:
Warnings for external use only. avoid contact with the eyes or broken skin.
Dosage and Administration:
Directions massage the cream daily into your butt with strong circling motions. to make the effect last, long term and repeated use is recommended.
Package Label Principal Display Panel:
44074 tu_lbl_perfect butt booster cream idrug facts_perfect butt booster creammage description