CHG- isopropyl alcohol swab

CHG by

Drug Labeling and Warnings

CHG by is a Otc medication manufactured, distributed, or labeled by Longood Medicine (Beijing) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl Alcohol 70%

Purpose

Purpose:

Antiseptic

Use

Use:

For preparation of the skin prior to injection, infusion, transfusion, and operation.

First aid to help prevent infection in minor cut, scrapes, abd burns

Warning

For external use only.

Do Not Use

Do not

● use in the eyes

● use on individuals who are allergic or sensitive to Chlorhexidine gluconate (CHG) and isopropyl alcohol (IPA)

Stop Use and Consult a Doctor

Stop Use and Consult a Doctor

●if the condition persists or gets worse

● for use longer than 1 week. Ask a doctor in case of deep or puncture wounds, animal bites, serious burns

Ask a doctor in case of deep or puncture wounds, animal bites, serious burns

Keep out of reach of children

Keep out of reach of children

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

Direction:

Directions

• Clean the affected area
• Apply the product to the area 1-3 times daily and discard.
• Maybe coverd with a sterile bandage when dry

Inactive Ingredient 

Inactive Ingredient:

Chlorhexidine Glutanate (2%), Purified water

Image of Pouch Label

INGREDIENTS AND APPEARANCE

CHG 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62382-0324
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62382-0324-1	0.2 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	08/28/2015
2	NDC: 62382-0324-2	0.3 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	08/28/2015
3	NDC: 62382-0324-3	0.4 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	08/28/2015
4	NDC: 62382-0324-4	0.5 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	08/28/2015
5	NDC: 62382-0324-5	0.6 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	08/28/2015
6	NDC: 62382-0324-6	0.67 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	08/28/2015
7	NDC: 62382-0324-7	1 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	08/28/2015
8	NDC: 62382-0324-8	1.5 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	08/28/2015
9	NDC: 62382-0324-9	1.75 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	08/28/2015
10	NDC: 62382-0324-0	3 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	08/28/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/28/2015

Labeler - Longood Medicine (Beijing) Co., Ltd. (529553064)

Establishment
Name	Address	ID/FEI	Business Operations
Longood Medicine (Beijing) Co., Ltd.		529553064	manufacture(62382-0324)