Lacto Pack D29 Cream Care
Lactobacillus Ferment
Gsl-bio Co.,ltd.
Human Otc Drug
NDC 82684-001Lacto Pack D29 Cream Care also known as Lactobacillus Ferment is a human otc drug labeled by 'Gsl-bio Co.,ltd.'. National Drug Code (NDC) number for Lacto Pack D29 Cream Care is 82684-001. This drug is available in dosage form of Soap. The names of the active, medicinal ingredients in Lacto Pack D29 Cream Care drug includes Lactobacillus Fermentum - .4 g/100g . The currest status of Lacto Pack D29 Cream Care drug is Active.
Drug Information:
| Drug NDC: | 82684-001 |
| 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: | Lacto Pack D29 Cream Care |
| 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: | Lactobacillus Ferment |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Gsl-bio Co.,ltd. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Soap |
| 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: | LACTOBACILLUS FERMENTUM - .4 g/100g
|
| 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 DRUG OTHER |
| 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: | 22 Apr, 2022 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 10 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: | GSL-BIO CO.,LTD.
|
| 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: | 8809438410229
|
| UPC stands for Universal Product Code. |
| UNII: | 2C1F12C6AP
|
| 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 |
|---|
| 82684-001-01 | 80 g in 1 BOX (82684-001-01) | 22 Apr, 2022 | 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 acne, anti-inflammatory
Product Elements:
Lacto pack d29 cream care lactobacillus ferment sodium palmate purslane activated charcoal sodium chloride etidronate tetrasodium limonene, (+/-)- sodium palm kernelate water houttuynia cordata flowering top lactobacillus fermentum lactobacillus fermentum glycerin lime (calcium oxide) hydrolyzed bovine elastin (base; 1000 mw) palm acid edetate sodium scutellaria baicalensis root asian ginseng jojoba oil buckminsterfullerene palm kernel acid linalool, (+/-)-
Indications and Usage:
Direction use daily on face, body and hair as well, for even better effectiveness of removing make up and wastes in pores. especially secondary cleansing has an effect in washing and tone up.
Warnings:
Warning store in a cool and dry place.
Dosage and Administration:
Use it helps to treatment of atopic dermatitis it helps to acne treatment it helps to skin's refreshing and sedation antibacterial, anti-inflammatory
Stop Use:
Stop use and ask a doctor if irritation and redness develops.
Package Label Principal Display Panel:
Package label 82684-001-01