CENTELLA ASIATICA

Manufacturer
Cho-A Pharm.Co.,Ltd.
Effective date
2019-02-22
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-02 00:30:38

Label at a glance#

ProductNo-SCAR Oint.
Active ingredientCENTELLA ASIATICA, NEOMYCIN SULFATE, HYDROCORTISONE ACETATE
Label structure8 sections

Indications and uses

Minor cuts Scrapes Burns

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Centella Titrated Extract 10mg

Hydrocortisone Acetate 10mg

Neomycin Sulfate 3.5 mg

Purpose

OTC - PURPOSE SECTION

Scar control

external analgesic

First Aid Antibiotic

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Uses

INDICATIONS & USAGE SECTION

Minor cuts

Scrapes

Burns

Warnings

WARNINGS SECTION

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.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Polyethylene glycol, White Petrolatum, Light Liquid Paraffin

No-SCAR Oint.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NOSCAROINTNOSCAROINT

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58354-11358354-113-01, 58354-113-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1b8d0909-b38a-1794-e063-6294a90a243782872a07-04db-5263-e053-2a91aa0aa2c22024-06-23WarningsExact identifier
spl set id: 82872a07-04db-5263-e053-2a91aa0aa2c2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.