NDC 58354-113 No-scar Oint.

Centella Titrated Extract Neomycin Sulfate, Hydrocortisone Acetate, Neomycin Sulfate

NDC Product Code 58354-113

NDC Code: 58354-113

Proprietary Name: No-scar Oint. 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: Centella Titrated Extract Neomycin Sulfate, Hydrocortisone Acetate, Neomycin Sulfate 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.

NDC Code Structure

  • 58354 - Cho-a Pharm.co.,ltd.
    • 58354-113 - No-scar Oint.

NDC 58354-113-02

Package Description: 1 TUBE in 1 CARTON > 10 g in 1 TUBE (58354-113-01)

NDC Product Information

No-scar Oint. with NDC 58354-113 is a a human over the counter drug product labeled by Cho-a Pharm.co.,ltd.. The generic name of No-scar Oint. is centella titrated extract neomycin sulfate, hydrocortisone acetate, neomycin sulfate. The product's dosage form is ointment and is administered via topical form.

Labeler Name: Cho-a Pharm.co.,ltd.

Dosage Form: Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >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.

No-scar Oint. 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.

  • NEOMYCIN SULFATE 3.5 mg/10g

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.


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: Cho-a Pharm.co.,ltd.
Labeler Code: 58354
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: 02-22-2019 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.

No-scar Oint. Product Label Images

No-scar Oint. 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

Centella Titrated Extract 10mgHydrocortisone Acetate 10mgNeomycin Sulfate 3.5 mg


Scar controlexternal analgesicFirst Aid Antibiotic

Keep Out Of Reach Of Children

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


Minor cutsScrapesBurns


For external use only.Ask a doctor before use in case of: Deep puncture wounds, Animal bites, Or serious burns
Do not use: if you are allergic to any of the ingredients, in the eyes, over large areas of the body, longer than 1 week unless directed by a doctor
Stop use and ask a doctor if: the condition worsens, or if symptoms persist for more than 7days or clear up and occur again within a few days.
Do not begin to use any other hydrocortisone product unless you have consulted a doctor.


Adults and children 2 years of age and older: apply to the affected area 1 to 2 times daily

Inactive Ingredients

Polyethylene glycol, White Petrolatum, Light Liquid Paraffin

* Please review the disclaimer below.

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