Ammonia Inhalants

Manufacturer: YOUNG DENTAL MANUFACTURING CO 1, LLC
Effective date: 2023-01-03
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-05-31 23:52:56

Label at a glance#

ProductAmmonia Inhalants

Active ingredientAMMONIA

Label structure8 sections

Dosage and administration

Directions: 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#

Actives

OTC - ACTIVE INGREDIENT SECTION

Ammonia 15 percent

Purpose

OTC - PURPOSE SECTION

Inhalant

Usage

INDICATIONS & USAGE SECTION

To treat or prevent fainting.

Warnings

WARNINGS SECTION

For External Use Only.

Stop use and ask a doctor if condition persists. Do not use if you have breathing problems such as asthma or emphysema.

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 immediately.

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

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

Inactives

INACTIVE INGREDIENT SECTION

Alcohol USP, FDC red dye 40, Lavender oil fcc, Lemon oil fcc, Nutmeg oil fcc, Purified water usp

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1299889	ammonia 15 % Nasal Inhalant	PSN	5
1299889	ammonia 150 MG/ML Nasal Inhalant	SCD	5
1299889	ammonia 0.045 GM per 0.3 ML Nasal Inhalant	SY	5
1299889	ammonia 0.3 ML Nasal Inhalant	SY	5
1299889	ammonia 15 % Nasal Inhalant	SY	5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0273-0104-10	2025-01-30	C162847	48780-1	2cef2736-89ba-d83d-e063-dadaa90ab31f	AMMONIA INHALER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0273-0104-10	Ammonia Inhalants	0.3 mL in 1 AMPULE	INHALANT	0.3		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0273-0104	AMMONIA INHALANTS INHALANT [YOUNG DENTAL MANUFACTURING CO 1, LLC]	5	Legacy NDC, 1 package rows	20230105_5d83b8c0-914c-4ad4-a1c6-45215bfacbd8.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Ammonia Inhalants
ALCOHOL
LEMON OIL
LAVANDIN OIL
NUTMEG OIL
FD&C RED NO. 40
WATER
AMMONIA

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0273-0104	0273-0104-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
LEMON OIL	I9GRO824LL	IACT
LAVANDIN OIL	9RES347CKG	IACT
NUTMEG OIL	Z1CLM48948	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
WATER	059QF0KO0R	IACT
AMMONIA	5138Q19F1X	ACTIB

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
f1621e06-f87b-2afa-e053-2a95a90a90e4			5d83b8c0-914c-4ad4-a1c6-45215bfacbd8	2023-01-03	Warnings	Exact identifier spl id: f1621e06-f87b-2afa-e053-2a95a90a90e4 spl set id: 5d83b8c0-914c-4ad4-a1c6-45215bfacbd8

Reported adverse events (FAERS/openFDA)#

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