Rescue Breather Kit

Manufacturer
Honeywell Safety Products USA, Inc | Changzhou Maokang Medical Products Co., Ltd
Effective date
2024-01-19
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
legacy-cache
Hydrated at
2026-08-01 21:13:50

Label at a glance#

ProductRescue Breather Kit
Active ingredientISOPROPYL ALCOHOL
Label structure10 sections

Indications and uses

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

Dosage and administration

clean the affected area may be covered with a sterile bandage

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire and flame

When using this product

OTC - WHEN USING SECTION

  • 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

OTC - STOP USE SECTION

  • the condition persists or gets worse

Keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredient

INACTIVE INGREDIENT SECTION

water

Questions

OTC - QUESTIONS SECTION

1-800430-5490

Alcohol Prep

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

alcohol prepalcohol prep

Rescue Breather Kit label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rescue BreatherRescue Breather

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0498-90000498-9000-01
0498-01410498-0141-04

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
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB

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
1a516d58-ceb0-59ed-e063-6394a90a065e61057c72-0927-7dff-e053-2a91aa0aac0b2024-06-07WarningsExact identifier
spl set id: 61057c72-0927-7dff-e053-2a91aa0aac0b

Reported adverse events (FAERS/openFDA)#

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