Cho-A Derm-R

Manufacturer: Cho-A Pharm.Co.,Ltd.
Effective date: 2021-12-06
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 22:24:43

Label at a glance#

ProductCho-A Derm-R

Active ingredientCARBOXYMETHYLCELLULOSE SODIUM

Label structure8 sections

Indications and uses

helps to reduce the risk of infection in minor cuts, scraps and burns.

Dosage and administration

Choose the right size of bandage to completely cover the affected area. Apply one patch at a time.

Contacts and useful links#

PhonePoison Help1-800-222-1222

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Carboxymethylcellulose Sodium (130mg) ------------------------------------------------- Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Directions

DOSAGE & ADMINISTRATION SECTION

Choose the right size of bandage to completely cover the affected area.

Apply one patch at a time.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylic ester copolymer, Polyurethane.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Warnings

WARNINGS SECTION

For external use only

Do not reuse

Stop use and consult a doctor if the condition persists or gets worse.

Do not use

Longer than one week unless directed by a physician. In case of deep or puncture wounds, animal bites or serious burn, consult a physician.

Uses

INDICATIONS & USAGE SECTION

helps to reduce the risk of infection in minor cuts, scraps and burns.

Cho-A Derm-R

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Cho-A Derm-R
Carboxymethylcellulose Sodium
POLYBUTENE (1400 MW)
CARBOXYMETHYLCELLULOSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
58354-121	58354-121-01, 58354-121-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
POLYBUTENE (1400 MW)	1NA5AO9GH7	IACT
CARBOXYMETHYLCELLULOSE SODIUM	K679OBS311	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
1b8cbcc7-f756-f632-e063-6394a90a3b59			d2805e95-338e-58cc-e053-2995a90acfd8	2024-06-23	Warnings	Exact identifier spl set id: d2805e95-338e-58cc-e053-2995a90acfd8

Reported adverse events (FAERS/openFDA)#

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