Ammonia Inhalants

Manufacturer
Dynarex Corporation
Effective date
2025-08-11
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:10:10

Label at a glance#

ProductAmmonia Inhalants
Active ingredientAMMONIA
Label structure9 sections

Storage and handling

Store at room temperature away from light

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

active ingredient each inhalant purpose ammonia 15% inhalant

OTC - PURPOSE SECTION

Uses to prevent or treating fainting

warnings 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

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

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

Store at room temperature away from light

INACTIVE INGREDIENT SECTION

alcohol fdc red dye 40 lavender oil, lemon oil, nutmeg oil, purified water usp

INDICATIONS & USAGE SECTION

to prevent or treat fainting

WARNINGS SECTION

for external use only

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1401 BX MASTER1401 BX MASTER1401 Ammonia Inhalants

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1299889ammonia 15 % Nasal InhalantPSN7
1299889ammonia 150 MG/ML Nasal InhalantSCD7
1299889ammonia 0.045 GM per 0.3 ML Nasal InhalantSY7
1299889ammonia 0.3 ML Nasal InhalantSY7
1299889ammonia 15 % Nasal InhalantSY7

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67777-251-01Ammonia Inhalants0.33 mL in 1 AMPULEINHALANT0.337
67777-251-01Ammonia Inhalants10 in 1 BOXINHALANT107
67777-251-02Ammonia Inhalants50 in 1 CASEINHALANT507

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67777-251-01EA - Each67777-25151618e6e-d56c-487c-8ab6-7deb570ed41b12018-06-11
67777-251-02EA - Each67777-2515ac0709d-edf2-41dc-9feb-b151a56bfaee12024-11-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ammoniaACTIVE INGREDIENT5138Q19F1X1
ammoniaACTIVE MOIETY5138Q19F1X1
alcoholINACTIVE INGREDIENT3K9958V90M1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67777-25167777-251-01, 67777-251-02

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
AMMONIA5138Q19F1XACTIB
ALCOHOL3K9958V90MIACT

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
alcoholALCOHOL3K9958V90MSOLUTION / RESPIRATORY (INHALATION)0.08 %w/vExact 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
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
alcoholALCOHOL3K9958V90MAEROSOL, SPRAY / RESPIRATORY (INHALATION)35.75 %w/wExact identifier — unii+route
12 equally ranked IID candidates
alcoholALCOHOL3K9958V90MAEROSOL, METERED / RESPIRATORY (INHALATION)26664 mgExact identifier — unii+route
12 equally ranked IID candidates
alcoholALCOHOL3K9958V90MLIQUID / RESPIRATORY (INHALATION)5 %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
alcoholALCOHOL3K9958V90MAEROSOL, SPRAY / RESPIRATORY (INHALATION)35.75 %w/wExact 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 INHALANTSDynarex Corporation91e27f1c-0f74-413e-97ff-2fc013f22ca82025-08-11WarningsExact identifier
ndc (package): 67777-251-02
ndc (package): 67777-251-01
ndc (product): 67777-251
ndc11 (package): 67777025102
ndc11 (package): 67777025101
spl id: 3c176ea9-62a1-b86f-e063-6294a90ab8f7
spl set id: 91e27f1c-0f74-413e-97ff-2fc013f22ca8

Reported adverse events (FAERS/openFDA)#

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