Pahaba Control
Niacinamide
Jh Science Co., Ltd.
Human Otc Drug
NDC 81715-0001Pahaba Control also known as Niacinamide is a human otc drug labeled by 'Jh Science Co., Ltd.'. National Drug Code (NDC) number for Pahaba Control is 81715-0001. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Pahaba Control drug includes Niacinamide - 5 g/100mL . The currest status of Pahaba Control drug is Active.
Drug Information:
| Drug NDC: | 81715-0001 |
| 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: | Pahaba Control |
| 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: | Niacinamide |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Jh Science Co., Ltd. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Liquid |
| 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: | NIACINAMIDE - 5 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 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: | 04 Apr, 2021 |
| 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: | JH Science 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. |
| UNII: | 25X51I8RD4
|
| 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 |
|---|
| 81715-0001-1 | 50 mL in 1 BOTTLE (81715-0001-1) | 04 Apr, 2021 | 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:
Strengthen the skin and protect the skin from harmful external environments making it healthy
Product Elements:
Pahaba control niacinamide niacinamide niacinamide water
Indications and Usage:
Every evening after a facial cleansing, apply pahaba control on your face and pat for more than 3 minutes for thorough absorption.
Warnings:
1) ask a dermatologist if there are any irritation or side effects such as red spots, swelling, and itching after using the cosmetics or being exposed to direct sunlight. 2) do not use on damaged or broken skin. 3) precautions for storage. a) keep away from children. b) keep away from direct sunlight. 4) α-hydroxyacid (aha) containing product a) use with sunblock because the product couldincrease skinâs sensitivity to the sunlight. b) test on some skin areas to check whether the product causes skin irritation. 5) do not use it for children under 3 years old.
Dosage and Administration:
External use only
Package Label Principal Display Panel:
Label