FDA.reportPublic FDA data

ammonia inhalants

Manufacturer
Epic Medical Supply Corp
Effective date
2024-09-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:18:42

Label at a glance#

Productammonia inhalants
Active ingredientAMMONIA
Label structure10 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.

KEEP OUT OF REACH OF CHILDREN

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagePackage

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagePackage

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1299889ammonia 15 % Nasal InhalantPSN1
1299889ammonia 150 MG/ML Nasal InhalantSCD1
1299889ammonia 0.045 GM per 0.3 ML Nasal InhalantSY1
1299889ammonia 0.3 ML Nasal InhalantSY1
1299889ammonia 15 % Nasal InhalantSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82749-150-01ammonia inhalants0.3 mL in 1 AMPULEINHALANT0.31
82749-150-02ammonia inhalants100 in 1 BOXINHALANT1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82749-150AMMONIA INHALANTS (INHALANT) INHALANT [EPIC MEDICAL SUPPLY CORP]1Current NDC, 2 package rows20240905_20e849e5-8517-b9fd-e063-6394a90a0d23.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82749-15082749-150-01, 82749-150-02

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
FD&C RED NO. 40WZB9127XOAIACT
AMMONIA5138Q19F1XACTIB
WATER059QF0KO0RIACT

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
ammonia inhalantsINHALANTEpic Medical Supply Corp20e849e5-8517-b9fd-e063-6394a90a0d232024-09-03WarningsExact identifier
ndc (package): 82749-150-01
ndc (package): 82749-150-02
ndc (product): 82749-150
ndc11 (package): 82749015002
ndc11 (package): 82749015001
spl id: 20e849e5-8518-b9fd-e063-6394a90a0d23
spl set id: 20e849e5-8517-b9fd-e063-6394a90a0d23

Reported adverse events (FAERS/openFDA)#

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