FDA.reportPublic FDA data

Ammonia Inhalent

Manufacturer
Honeywell Safety Products USA, Inc | NORTH SAFETY DE MEXICALI, S. DE R.I. DE C.V.
Effective date
2021-12-09
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
legacy-cache
Hydrated at
2026-08-01 22:23:46

Label at a glance#

ProductNorth Ammonia Inhalent
Active ingredientAMMONIA
Label structure10 sections

Indications and uses

to prevent or treat fainting

Dosage and administration

hold inhalant away from face and crush ampoule between thumb and forefinger at position indicated on sleeve. hold near nostrils for inhalation of volatile vapor

Label contents#

Full prescribing information#

Active ingredient (in each ampoule)

OTC - ACTIVE INGREDIENT SECTION

Ammonia 15%

Purpose

OTC - PURPOSE SECTION

Respiratory stimulant

Uses

INDICATIONS & USAGE SECTION

to prevent or treat fainting

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • if you have breathing problems such as asthma or emphysema

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition persists

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • hold inhalant away from face and crush ampoule between thumb and forefinger at position indicated on sleeve.
  • hold near nostrils for inhalation of volatile vapor

Other information

SPL UNCLASSIFIED SECTION

store at room temperature away from light

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol USP, FD&C red #40, lavender oil, lemon oil fcc, nutmeg oil, purified water

Questions or comments?

OTC - QUESTIONS SECTION

1-800-430-5490

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ammonia inhalantammonia inhalant

Honeywell Ammonia

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Honeywell AmmoniaHoneywell Ammonia

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
0498-33340498-3334-00, 0498-3334-34
0498-33330498-3333-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
AMMONIA5138Q19F1XACTIB
ALCOHOL3K9958V90MIACT
AMMONIA5138Q19F1XACTIB

Source Document#

Source XML · Source PDF

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
0ecac20c-a32d-f021-e063-6394a90ae13960020385-796e-050b-e053-2991aa0a1a722024-01-12WarningsExact identifier
spl set id: 60020385-796e-050b-e053-2991aa0a1a72

Reported adverse events (FAERS/openFDA)#

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