NO-SCAR OINT.- centella titrated extract neomycin sulfate, hydrocortisone acetate, neomycin sulfate ointment

No-SCAR Oint. by

Drug Labeling and Warnings

No-SCAR Oint. by is a Otc medication manufactured, distributed, or labeled by Cho-A Pharm.Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Centella Titrated Extract 10mg

Hydrocortisone Acetate 10mg

Neomycin Sulfate 3.5 mg

Purpose

Scar control

external analgesic

First Aid Antibiotic

Keep out of reach of children

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

Uses

Minor cuts

Scrapes

Burns

Warnings

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

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

No-SCAR Oint.

INGREDIENTS AND APPEARANCE

NO-SCAR OINT. 
centella titrated extract neomycin sulfate, hydrocortisone acetate, neomycin sulfate ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58354-113
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CENTELLA ASIATICA (UNII: 7M867G6T1U) (CENTELLA ASIATICA - UNII:7M867G6T1U)	CENTELLA ASIATICA	10 mg  in 10 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN SULFATE	3.5 mg  in 10 g
HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE ACETATE	10 mg  in 10 g

Inactive Ingredients
Ingredient Name	Strength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)	70 mg  in 10 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58354-113-02	1 in 1 CARTON	02/22/2019
1	NDC: 58354-113-01	10 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/22/2019

Labeler - Cho-A Pharm.Co.,Ltd. (688056831)

Registrant - Cho-A Pharm.Co.,Ltd. (688056831)

Establishment
Name	Address	ID/FEI	Business Operations
Cho-A Pharm.Co.,Ltd.		688056831	manufacture(58354-113)