NDC 73430-0006 Dr.nuell Water Full Skin Barrier Losesnce

Glycerin, Adenosine

NDC Product Code 73430-0006

NDC CODE: 73430-0006

Proprietary Name: Dr.nuell Water Full Skin Barrier Losesnce 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: Glycerin, 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.

  • This product is used to relieve occasional constipation. Glycerin belongs to a class of drugs known as hyperosmotic laxatives. It works by drawing water into the intestines. This effect usually results in a bowel movement within 15 to 60 minutes. For adults, the normal frequency of bowel movements varies from once daily to 1 to 2 times weekly. For preschool-aged children, the normal frequency of bowel movements varies from once daily to once every other day. Constipation is best treated by drinking plenty of fluids, eating foods high in fiber, and exercising regularly.
  • Drug uses not available

NDC Code Structure

  • 73430 - Apharm Co., Ltd.
    • 73430-0006 - Dr.nuell Water Full Skin Barrier Losesnce

NDC 73430-0006-1

Package Description: 150 mL in 1 PACKAGE

NDC Product Information

Dr.nuell Water Full Skin Barrier Losesnce with NDC 73430-0006 is a a human over the counter drug product labeled by Apharm Co., Ltd.. The generic name of Dr.nuell Water Full Skin Barrier Losesnce is glycerin, adenosine. The product's dosage form is cream and is administered via topical form.

Labeler Name: Apharm Co., Ltd.

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Dr.nuell Water Full Skin Barrier Losesnce 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.

  • GLYCERIN .59095 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.

  • ALLANTOIN (UNII: 344S277G0Z)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

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: Apharm Co., Ltd.
Labeler Code: 73430
FDA Application Number: part347 What 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. 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: 11-01-2019 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: 12-31-2020 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.

Dr.nuell Water Full Skin Barrier Losesnce Product Label Images

Dr.nuell Water Full Skin Barrier Losesnce 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, adenosine

Otc - Purpose

Wrinkle improving functional products.premium wrinkle lotion for face, improving skin elasticity

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

Take an appropriate amount and apply it on the face and neck along the skin texture, then, pat it until fully absorbed

Warnings

1) if there is any abnormal symptom or side effect, such as red spot, swelling and itching when using cosmetlcs or after using due to direct sunlight, consult dermatologists

2) Do not use for wounded areas

3) Precautions for storage and handling

keep out of reach of children, store away from direct sunlight

4) avoid the eye area

Inactive Ingredient

SEA WATER

PANTHENOL

BUTYLENE GLYCOL

PENTYLENE GLYCOL

NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE

C12-15 ALKYL BENZOATE

SANGUISORBA OFFICINALIS ROOT EXTRACT

HYDROLYZED COLLAGEN

CENTELLA ASIATICA EXTRACT

ACETYL HEXAPEPTIDE-8

ALLANTOIN

SODIUM HYALURONATE

CERAMIDE 3

HYDROGENATED LECITHIN

MADECASSOSIDE

CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT

GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT

CINNAMOMUM CASSIA BARK EXTRACT

ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT

GLYCINE SOJA (SOYBEAN) SPROUT EXTRACT

PLANKTON EXTRACT

C14-22 ALCOHOLS

1,2-HEXANEDIOL

CETYL ETHYLHEXANOATE

GLYCERYL STEARATE SE

HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER

AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER

C12-20 ALKYL GLUCOSIDE

HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL

CAPRYLYL GLYCOL

CAPRYLIC/CAPRIC TRIGLYCERIDE

WATER

CITRUS PARADISI (GRAPEFRUIT) PEEL OIL

LITSEA CUBEBA FRUIT OIL

PELARGONIUM GRAVEOLENS FLOWER OIL

SALVIA OFFICINALIS (SAGE) OIL

DISODIUM EDTA

Dosage & Administration

For external use only

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