Resurfix Plus
Petrolatum
Topiderm, Inc.
Human Otc Drug
NDC 51326-884Resurfix Plus also known as Petrolatum is a human otc drug labeled by 'Topiderm, Inc.'. National Drug Code (NDC) number for Resurfix Plus is 51326-884. This drug is available in dosage form of Ointment. The names of the active, medicinal ingredients in Resurfix Plus drug includes Petrolatum - 86 mg/g . The currest status of Resurfix Plus drug is Active.
Drug Information:
| Drug NDC: | 51326-884 |
| 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: | Resurfix Plus |
| 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: | Petrolatum |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Topiderm, Inc. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Ointment |
| 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: | PETROLATUM - 86 mg/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 Jan, 2000 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 15 Jun, 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: | 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, 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: | Topiderm, Inc.
|
| 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: | 0358211884354
|
| UPC stands for Universal Product Code. |
| UNII: | 4T6H12BN9U
|
| 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 |
|---|
| 51326-884-03 | 100 g in 1 TUBE (51326-884-03) | 01 Jan, 2000 | 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:
Resurfix plus petrolatum petrolatum petrolatum allantoin benzyl alcohol green tea leaf ceramide ng ceramide np alkyl (c12-15) benzoate ethylhexyl palmitate soybean lanolin alcohols mineral oil palmitoyl tripeptide-1 panthenol peg-10 rapeseed sterol lecithin, soybean saccharomyces lysate sorbitan isostearate squalane .alpha.-tocopherol acetate tribehenin yucca glauca root water
Indications and Usage:
Uses a unique dressing formulated to aid in the skin barrier healing process. also provides protection and helps heal stressed skin conditions such as chapped, dry and windburned skin.
Warnings:
Warnings not to be applied over puncture wounds, infections, or lacerations. if condition worsens or does not improve within 7 days, contact a physician. keep out of reach of children. in case of accidental ingestion, seek professional assistance or contact a poison control center immediately. for external use only, not to be swallowed. avoid contact with eyes.
Dosage and Administration:
Directions apply as directed by your physician.
Package Label Principal Display Panel:
Principal display panel - 100 g tube label replenix ® resurfix + skin barrier healing ointment skin protectant post aesthetic ⢠post procedure ⢠post treatment ceramide 2 & 3 ⢠lycd green tea extract ⢠squalane nf panthenol ⢠vitamin e ⢠allantoin petrolatum usp net wt. 3.5 oz. (100 g.) topix pharmaceuticals, inc. ⢠n. amityville, ny 11701 principal display panel - 100 g tube label