RESCUE BREATHER KIT- isopropyl alcohol kit

Rescue Breather Kit by

Drug Labeling and Warnings

Rescue Breather Kit by is a Otc medication manufactured, distributed, or labeled by Honeywell Safety Products USA, Inc, Changzhou Maokang Medical Products Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Isopropyl alcohol 70%

Purpose

First aid antiseptic

Uses

first aid to help prevent infection in minor cuts, scrapes, and burns

Warnings

For external use only

Flammable, keep away from fire and flame

When using this product

• do not use in the eyes
• do not apply over large areas of the body
• do not use longer than 1 week unless directed by a doctor
• do not use in case of deep or puncture wounds, animal bites, or serious burns
  

Stop use and consult a doctor if

• the condition persists or gets worse
  

Keep out of the reach of children

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

Directions

• clean the affected area
• may be covered with a sterile bandage
  

Other information

store at room temperature 15 o to 25 o C (59 o to 77 oF)

Inactive ingredient

water

Questions

1-800430-5490

Alcohol Prep

Rescue Breather Kit label

INGREDIENTS AND APPEARANCE

RESCUE BREATHER KIT 
isopropyl alcohol kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0498-9000

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0498-9000-01	4 in 1 KIT	01/01/2017
1		1 in 1 POUCH; Type 0: Not a Combination Product

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	3 POUCH	1 mL

Part 1 of 1

NORTH ALCOHOL WIPE 
isopropyl alcohol swab

Product Information
Item Code (Source)	NDC: 0498-0141
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0498-0141-04	0.4 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/23/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2017

Labeler - Honeywell Safety Products USA, Inc (079287321)

Registrant - Honeywell Safety Products USA, Inc (079287321)

Establishment
Name	Address	ID/FEI	Business Operations
Honeywell Safety Products USA, Inc		079287321	manufacture(0498-9000) , pack(0498-0141)

Establishment
Name	Address	ID/FEI	Business Operations
Changzhou Maokang Medical Products Co., Ltd		421317073	manufacture(0498-0141)