NDC 72575-102 Repairing And Soothing Treatment Essence


NDC Product Code 72575-102

NDC 72575-102-02

Package Description: 1 BOTTLE, SPRAY in 1 BOX > 100 g in 1 BOTTLE, SPRAY (72575-102-01)

NDC Product Information

Repairing And Soothing Treatment Essence with NDC 72575-102 is a a human over the counter drug product labeled by Vesen, Inc. The generic name of Repairing And Soothing Treatment Essence is allantoin. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Vesen, Inc

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.

Repairing And Soothing Treatment Essence 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.

  • ALLANTOIN .5 g/100g

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.
  • 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: Vesen, Inc
Labeler Code: 72575
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 FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. 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: 08-16-2019 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.

Repairing And Soothing Treatment Essence Product Label Images

Repairing And Soothing Treatment Essence 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 Ingredients



Skin Protectant

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.


Soothe irritated and compromised skin, Promote the renewal of skin

Inactive Ingredients

Water, Propandiol, Glycerin, Betaine, Centella Asiatica (Gotu Kola) Leaf Extract, Salix Nigra (Willow) Bark extract, 1,2 hexandiol and Caprylyl glycol, Sodium Phytate, Citric acid.


For external use onlyDo not use when skin is red, inflamed, irritated, or painfulWhen using this productAvoid contact with eyes. If contact occurs, rinse eyes thoroughly with waterStop use and ask a doctor ifRash or irritation on skin develops and lasts


Shake gently before use. After cleaning, apply daily, morning and evening (or as needed) all over the face. Massage gently with fingertips until it is absorbed or saturate cotton pads in essence and apply to area of concern, leave on for 10-15 min.

* Please review the disclaimer below.