NDC 72943-0003 Non-sheet Serumst

Glycerin, Allantoin

NDC Product Code 72943-0003

NDC Product Information

Non-sheet Serumst with NDC 72943-0003 is a a human over the counter drug product labeled by Daonmedicos Co.. The generic name of Non-sheet Serumst is glycerin, allantoin. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Daonmedicos Co.

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 Additional informationCallout TooltipWhat 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.


Non-sheet Serumst Active Ingredient(s)

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

  • GLYCERIN 3 g/100mL

Inactive Ingredient(s)

Additional informationCallout TooltipAbout 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.

  • WATER (UNII: 059QF0KO0R)
  • ALLANTOIN (UNII: 344S277G0Z)

Administration Route(s)

Additional informationCallout TooltipWhat 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.

Product Labeler Information

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Daonmedicos Co.
Labeler Code: 72943
FDA Application Number: part347 Additional informationCallout TooltipWhat is the FDA Application Number?
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.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. Additional informationCallout TooltipWhat 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: 03-24-2019 Additional informationCallout TooltipWhat 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: 12-31-2020 Additional informationCallout TooltipWhat 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 Additional informationCallout TooltipWhat 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.

Non-sheet Serumst Product Label Images

Non-sheet Serumst 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

Otc - Active Ingredient

GLYCERIN

Inactive Ingredient

Sea Water

Water

Butylene Glycol

Glycerin

Niacinamide

Saccharomyces/Artemisia Princeps Leaf Ferment Filtrate

Elaeagnus Glabra Extract

Pentylene Glycol

Hexacarboxymethyl Dipeptide-12

Dipotassium Glycyrrhizate

Gellan Gum

rh-Oligopeptide-1

sh-Decapeptide-7

sh-Octapeptide-4

sh-Oligopeptide-9

sh-Pentapeptide-19

Digalloyl Tetrapeptide-19

Tripeptide-48

Nicotinoyl Tripeptide-1

Palmitoyl Pentapeptide-4

Ovalicin

Propanediol

Nonapeptide-29 Hexapeptide-8

Nonapeptide-29 Pentapeptide-4

Isopentyldiol

Polyglyceryl-4 Oleate

Sucrose Palmitate

Ceramide NP

Propanediol

Butylene Glycol

Portulaca Oleracea Extract

Centella Asiatica Extract

Adenosine

Disodium EDTA

Allantoin

Panthenol

Betaine

Sodium Chloride

Water

Human Adipocyte Conditioned Media Extract

Phytosphingosine

Ceramide NP

Phospholipids

Caprylyl Glycol

Tropolone

Phytosterols

Squalane

1,2-Hexanediol

Otc - Purpose

Whiteninganti-wrinkle

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Spread evenly over the skin

Warnings

■ if following abnormal symptoms occurs after use , stop use and consult with a skin specialistred specks, swelling, itching■ don’t use on the part where there is injury, eczema, or dermatitisKeep out of reach of children■ if swallowed, get medical help or contact a person control center immediately

Dosage & Administration

For external use only

* Please review the disclaimer below.

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