Neat 3b Bodysaver
Skin Protectant
Neat Feat Products Limited
Human Otc Drug
NDC 50017-022Neat 3b Bodysaver also known as Skin Protectant is a human otc drug labeled by 'Neat Feat Products Limited'. National Drug Code (NDC) number for Neat 3b Bodysaver is 50017-022. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in Neat 3b Bodysaver drug includes Zinc Acetate - .15 g/75g . The currest status of Neat 3b Bodysaver drug is Active.
Drug Information:
| Drug NDC: | 50017-022 |
| 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: | Neat 3b Bodysaver |
| 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: | Skin Protectant |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Neat Feat Products Limited |
| 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: | ZINC ACETATE - .15 g/75g
|
| 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 Jan, 2023 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 18 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. |
| Application Number: | part347 |
| 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: | Neat Feat Products Limited
|
| 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: | 0705102201309
|
| UPC stands for Universal Product Code. |
| UNII: | FM5526K07A
|
| 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. |
| Pharmacologic Class: | Copper Absorption Inhibitor [EPC]
Decreased Copper Ion Absorption [PE]
|
| These are the reported pharmacological class categories corresponding to the SubstanceNames listed above. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 50017-022-04 | 1 TUBE in 1 BOX (50017-022-04) / 75 g in 1 TUBE (50017-022-03) | 01 Jan, 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:
Purpose skin protectant
Product Elements:
Neat 3b bodysaver skin protectant propylparaben aluminum chlorohydrate mineral oil water propylene glycol glyceryl monostearate methylparaben peg-100 stearate cetostearyl alcohol petrolatum cetyl alcohol peg-40 stearate lanolin sorbitan monostearate diazolidinyl urea zinc acetate zinc cation
Indications and Usage:
Uses helps prevent and temporarily protects chafed skin between and beneath the breasts, buttocks and legs
Warnings:
Warnings for external use only do not use on an area that is infected and/or bleeding chafing due to deep puncture wounds, animal bites and/or serious burns when using this product keep out of eyes and mouth stop use and ask a doctor if rash, irritation or sensitivity develops chafing conditions worsen symptoms last more than 7 days or clear up and occur again within 7 days keep out of reach of children if swallowed, get medical help or contact a poison control center right away children under 2: ask a doctor
Do Not Use:
Warnings for external use only do not use on an area that is infected and/or bleeding chafing due to deep puncture wounds, animal bites and/or serious burns when using this product keep out of eyes and mouth stop use and ask a doctor if rash, irritation or sensitivity develops chafing conditions worsen symptoms last more than 7 days or clear up and occur again within 7 days keep out of reach of children if swallowed, get medical help or contact a poison control center right away children under 2: ask a doctor
When Using:
When using this product keep out of eyes and mouth
Dosage and Administration:
Directions shake well before use apply a dab to the palms of the hands rub between and beneath the breasts, buttocks and legs as needed.
Stop Use:
Stop use and ask a doctor if rash, irritation or sensitivity develops chafing conditions worsen symptoms last more than 7 days or clear up and occur again within 7 days
Package Label Principal Display Panel:
Principal display panel - 75 g tube box neat® 3b body saver cream no.1 australia's no.1 selling preventative cream for chafing fragrance free helps prevent skin chafing between & beneath the breasts buttocks & legs www.neatfeat.com active ingredient: zinc acetate (0.2%) 2.6 oz (75g) principal display panel - 75 g tube box
Further Questions:
Questions? call: 310 8344800