Ammonia Inhalants

Manufacturer
James Alexander Corporation
Effective date
2019-01-31
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:58:29

Label at a glance#

ProductAmmonia Inhalants
Active ingredientAMMONIA
Label structure12 sections

Indications and uses

To prevent or treat fainting.

Dosage and administration

Hold inhalant away from face and crush between thumb and forefinger. Carefully approach crushed inhalant to nostrils of affected person.

Label contents#

Full prescribing information#

Active Ingredients (each inhalant)

OTC - ACTIVE INGREDIENT SECTION

Ammonia (15%)

Purpose

OTC - PURPOSE SECTION

inhalant

Uses

INDICATIONS & USAGE SECTION

To prevent or treat fainting.

Warnings

WARNINGS SECTION

For external use only.

Do not use if you have breathing problems such as asthma or emphysema.

Stop use and ask a doctor if condition persists.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Hold inhalant away from face and crush between thumb and forefinger. Carefully approach crushed inhalant to nostrils of affected person.

Other Information

OTHER SAFETY INFORMATION

Store at room temperature away from light.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Alcohol USP, FD&C Red Dye # 40, Lavender Oil FCC, Lemon Oil FCC, Nutmeg Oil FCC, Purified Water USP.

Questions?

OTC - QUESTIONS SECTION

Call 1-908-362-9266 Monday through Friday. 9:00am - 5:00pm e.s.t

SPL UNCLASSIFIED SECTION

DISPENSING SOLUTIONS®


JAMES ALEXANDER CORPORATION
Blairstown, NJ• (908) 362-9266
Product information and MSDS available on-line at:
www.james-alexander.com

Void of Aqueous

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1299889ammonia 15 % Nasal InhalantPSN4
1299889ammonia 150 MG/ML Nasal InhalantSCD4
1299889ammonia 0.045 GM per 0.3 ML Nasal InhalantSY4
1299889ammonia 0.3 ML Nasal InhalantSY4
1299889ammonia 15 % Nasal InhalantSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
46414-3333-2Ammonia Inhalants100 in 1 CARTONINHALANT1004
46414-3333-3Ammonia Inhalants0.3 mL in 1 AMPULEINHALANT0.34

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
46414-3333AMMONIA INHALANTS INHALANT [JAMES ALEXANDER CORPORATION]4Current NDC, Legacy NDC, 2 package rows20190208_b741afa6-e56c-4fbb-ada0-80b80aef72a7.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AmmoniaACTIVE INGREDIENT5138Q19F1X3
AmmoniaACTIVE MOIETY5138Q19F1X3
AlcoholINACTIVE INGREDIENT3K9958V90M3

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
46414-333346414-3333-3, 46414-3333-2

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
AMMONIA5138Q19F1XACTIB
ALCOHOL3K9958V90MIACT
FD&C RED NO. 40WZB9127XOAIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 12 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
AlcoholALCOHOL3K9958V90MLIQUID / RESPIRATORY (INHALATION)5 %w/wExact identifier — unii+route
12 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MAEROSOL, SPRAY / RESPIRATORY (INHALATION)35.75 %w/wExact identifier — unii+route
12 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSOLUTION / RESPIRATORY (INHALATION)0.08 %w/vExact identifier — unii+route
12 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MAEROSOL, METERED / RESPIRATORY (INHALATION)26664 mgExact identifier — unii+route
12 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSOLUTION / RESPIRATORY (INHALATION)0.08 %w/vExact identifier — unii+route
12 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MAEROSOL, METERED / RESPIRATORY (INHALATION)26664 mgExact identifier — unii+route
12 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSOLUTION / RESPIRATORY (INHALATION)0.08 %w/vExact identifier — unii+route
12 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MLIQUID / RESPIRATORY (INHALATION)5 %w/wExact identifier — unii+route
12 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MAEROSOL, SPRAY / RESPIRATORY (INHALATION)35.75 %w/wExact identifier — unii+route
12 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MAEROSOL, SPRAY / RESPIRATORY (INHALATION)35.75 %w/wExact identifier — unii+route
12 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MLIQUID / RESPIRATORY (INHALATION)5 %w/wExact identifier — unii+route
12 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MAEROSOL, METERED / RESPIRATORY (INHALATION)26664 mgExact identifier — unii+route
12 equally ranked IID candidates

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
Ammonia InhalantsAMMONIA INHALANTSJames Alexander Corporationb741afa6-e56c-4fbb-ada0-80b80aef72a72019-01-31WarningsExact identifier
ndc (package): 46414-3333-2
ndc (package): 46414-3333-3
ndc (product): 46414-3333
ndc11 (package): 46414333303
ndc11 (package): 46414333302
spl id: a4d241dd-e857-4978-9112-0463a1fcf7d2
spl set id: b741afa6-e56c-4fbb-ada0-80b80aef72a7

Reported adverse events (FAERS/openFDA)#

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