NDC 72289-0005 Sandawha Moisturizing Baby


NDC Product Code 72289-0005

NDC 72289-0005-1

Package Description: 200 mL in 1 BOTTLE

NDC Product Information

Sandawha Moisturizing Baby with NDC 72289-0005 is a a human over the counter drug product labeled by Skincure Inc. The generic name of Sandawha Moisturizing Baby is glycerin. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Skincure Inc

Dosage Form: Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2

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.

Sandawha Moisturizing Baby 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 4.305 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.

  • WATER (UNII: 059QF0KO0R)

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.

Product Labeler Information

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

Labeler Name: Skincure Inc
Labeler Code: 72289
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: 02-24-2019 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.

Sandawha Moisturizing Baby Product Label Images

Sandawha Moisturizing Baby 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


Inactive Ingredient


Caprylic/Capric Triglyceride


Camellia Japonica Seed Oil

Hydrogenated Palm Kernel Oil

Pentylene Glycol



Phytosteryl Macadamiate


Camellia Sinensis Leaf Extract

Chamomilla Recutita (Matricaria) Leaf Extract

Thujopsis Dolabrata Branch Extract

Butyrospermum Parkii (Shea) Butter

Mangifera Indica (Mango) Seed Butter

Xanthan Gum

Sorbitan Caprylate

Glycyrrhiza Glabra (Licorice) Root Extract



Magnolia Kobus Bark Extract

Salix Alba (Willow) Bark Extract

Olea Europaea (Olive) Fruit Oil

Centella Asiatica Extract



Opuntia Ficus-Indica Fruit Extract

Dipotassium Glycyrrhizate


Aloe Barbadensis Leaf Extract

Dimethyl Sulfone

Polygonum Cuspidatum Root Extract

Scutellaria Baicalensis Root Extract

Citrus Unshiu Peel Extract

Rosmarinus Officinalis (Rosemary) Leaf Extract


Hyaluronic Acid

Rosa Canina Fruit Oil

Vitis Vinifera (Grape) Skin Extract

Stearyl Glycyrrhetinate


Houttuynia Cordata Extract

Linoleic Acid

Portulaca Oleracea Extract

Pyrus Malus (Apple) Fruit Extract

Silybum Marianum Extract

Vaccinium Angustifolium (Blueberry) Fruit Extract

Panax Ginseng Root Extract

Levulinic Acid

Ginkgo Biloba Leaf Extract

Morus Alba Bark Extract

Rubus Idaeus (Raspberry) Fruit Extract

Brassica Oleracea Italica (Broccoli) Extract

Glycine Soja (Soybean) Seed Extract

Pueraria Lobata Root Extract




Aniba Rosodora (Rosewood) Wood Oil

Jasminum Sambac (Jasmine) Flower Extract

Lavandula Angustifolia (Lavender) Oil

Rosmarinus Officinalis (Rosemary) Leaf Oil

Otc - Purpose

Soothes and protects sensitive skin

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Gently massage into skin as often as needed


For external use onlydo not use if sensitive to any of the ingredientsdiscontinue use if signs of irritation or rash appearif irritation or rash persists, contact a doctor

Dosage & Administration

For external use only

* Please review the disclaimer below.

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