NDC 76731-208 Stem Cell Hmsc Cell Rejuvenation-ampoule

Niacinamide, Adenosine

NDC Product Code 76731-208

NDC CODE: 76731-208

Proprietary Name: Stem Cell Hmsc Cell Rejuvenation-ampoule What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Niacinamide, Adenosine What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Niacinamide (nicotinamide) is a form of vitamin B3 (niacin) and is used to prevent and treat niacin deficiency (pellagra). Niacin deficiency can cause diarrhea, confusion (dementia), tongue redness/swelling, and peeling red skin. Niacinamide is often used instead of niacin because it causes fewer side effects (e.g., flushing). Unlike niacin, niacinamide does not help correct blood fat levels and cannot be substituted for niacin if you are being treated for a blood fat problem (e.g., high cholesterol). Niacin deficiency may happen as a result of poor diet, certain medical conditions (e.g., alcohol abuse, malabsorption syndrome, Hartnup disease), or long-term use of certain medications (e.g., isoniazid). It is best to get your vitamins from healthy foods. A multivitamin may be recommended by your doctor instead of niacinamide because poor diet usually causes deficiencies in more than one vitamin. Vitamins help to support the body's ability to make and break down natural substances (metabolism) and are needed for good health.
  • Drug uses not available

NDC Code Structure

  • 76731 - Bbhc Co., Ltd
    • 76731-208 - Stem Cell Hmsc Cell Rejuvenation-ampoule

NDC 76731-208-01

Package Description: 70 mL in 1 AMPULE

NDC Product Information

Stem Cell Hmsc Cell Rejuvenation-ampoule with NDC 76731-208 is a a human over the counter drug product labeled by Bbhc Co., Ltd. The generic name of Stem Cell Hmsc Cell Rejuvenation-ampoule is niacinamide, adenosine. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Bbhc Co., Ltd

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Stem Cell Hmsc Cell Rejuvenation-ampoule Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • NIACINAMIDE 2 g/100mL
  • ADENOSINE .04 g/100mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CANANGA OIL (UNII: 8YOY78GNNX)
  • 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
  • MAGNESIUM ASPARTATE (UNII: R17X820ROL)
  • CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
  • WATER (UNII: 059QF0KO0R)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • POLYGLYCERYL-10 OLEATE (UNII: 55C81W76DH)
  • AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
  • HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
  • SUCROSE DISTEARATE (UNII: 33X4X4B90S)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
  • COPPER GLUCONATE (UNII: RV823G6G67)
  • ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Bbhc Co., Ltd
Labeler Code: 76731
Marketing Category: UNAPPROVED DRUG OTHER - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/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.

Start Marketing Date: 10-31-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Stem Cell Hmsc Cell Rejuvenation-ampoule Product Label Images

Stem Cell Hmsc Cell Rejuvenation-ampoule Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Niacinamide (2.00%)Adenosine (0.04%)

Purpose

Skin BrighteningAnti wrinkle

Uses

  • Helps improve skin brightness and wrinkle care.Helps improve skin elasticity.

Warnings

For external use only

Do Not Use

On damaged or broken skin.

When Using This Product

Keep out of eyes. Rinse with water to remove.

Stop Use And Ask A Doctor If

Rash occurs.

Keep Out Of Reach Of Children.

If products is swallowed, get medical help or contact a Poison Control Center right away.

Directions

1) Wash your face thoroughly. Remove all makeups.2) Directly apply the ampoule on your towel-dried face.3) Remove the protection film from the bottle and screw open the lid.4) Remove the innerprotection film in the container/bottle, insert the easy squirt, and remove the top silver lid and apply the ampoule on any intended area.5) Allow enough amount of ampoule to get absorbed completely.

Inactive Ingredients

Human Umbilical Mesenchymal Stem Cell Conditioned Media, Glycerin, 1,2-Hexanediol, Caprylic/Capric Triglyceride, Cetyl Ethylhexanoate, Water, Glyceryl Acrylate/Acrylic Acid Copolymer, Propylene Glycol, Hydrogenated Lecithin, Polyglyceryl-10 Oleate, Sucrose Distearate, Ammonium Acryloyldimethyltaurate/VP Copolymer, Propanediol, Caprylhydroxamic Acid, Sodium Hyaluronate, DNA, Carbomer, Sodium Chloride, Magnesium Aspartate, Zinc Gluconate, Copper Gluconate, Glucose, Cananga Odorata Flower Oil

* Please review the disclaimer below.