Label at a glance#

ProductAmmonia Inhalants

Active ingredientAMMONIA

Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Ammonia 15%

OTC - PURPOSE SECTION

Purpose:

Reflex Stimulant

INDICATIONS & USAGE SECTION

Uses:

to aid in prevention and treatment of fainting

WARNINGS SECTION

Warnings:

For external use only

Flammable, keep away from heat or flame

OTC - DO NOT USE SECTION

Do not use:

if face is flush
in or near the eyes
if you have breathing problems such as asthma or emphysema

OTC - STOP USE SECTION

Stop use and ask a doctor if:

patient is non-responsive
condition lasts

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. 1-800-1222

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older:

hold away from face and crush inhalant between fingers
hold packet six inches from patient's nose
gradually move inhalant closer until patient revives
check strength frequently by holding near your own nose
if necessary, use another when first is expended
dispose of properly

Children under 12 years of age: ask a doctor

INACTIVE INGREDIENT SECTION

Inactive ingredients: alcohol USP, FD&C red dye #40, lavender oil FCC, lemon oil FCC, nutmeg oil FCC, purified water USP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0510ammoniav20f.jpg

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1299889	Ammonia (Nasal)	ammonia 150 MG/ML Nasal Inhalant	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1299889	ammonia 15 % Nasal Inhalant	PSN	1
1299889	ammonia 150 MG/ML Nasal Inhalant	SCD	1
1299889	ammonia 0.045 GM per 0.3 ML Nasal Inhalant	SY	1
1299889	ammonia 0.3 ML Nasal Inhalant	SY	1
1299889	ammonia 15 % Nasal Inhalant	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50332-0054-1	2023-01-30	C162847	48780-1	f386c649-bcf8-0266-e053-dadaa90a7c1a	d60287b7-7b65-4bd2-92ca-c87047ef9892

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50332-0054-1	Ammonia Inhalants	10 in 1 BOX	INHALANT	10		1
50332-0054-1	Ammonia Inhalants	.15 g in 1 AMPULE	INHALANT	.15		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50332-0054	AMMONIA INHALANTS (AMMONIA) INHALANT [HART HEALTH]	1	Legacy NDC, 2 package rows	20210523_d60287b7-7b65-4bd2-92ca-c87047ef9892.zip

Products#

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

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

Ammonia Inhalants
ammonia
ALCOHOL
FD&C RED NO. 40
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50332-0054	50332-0054-1

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
Name	UNII	Kind
AMMONIA	5138Q19F1X	ACTIB
ALCOHOL	3K9958V90M	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
236fade9-2ff7-46fe-b629-bd918f27aa0b			d60287b7-7b65-4bd2-92ca-c87047ef9892	2021-01-04	Warnings	Exact identifier spl id: 236fade9-2ff7-46fe-b629-bd918f27aa0b spl set id: d60287b7-7b65-4bd2-92ca-c87047ef9892

Reported adverse events (FAERS/openFDA)#

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

Ammonia Inhalants