Label at a glance#

ProductAmmoniaSport RAW

Active ingredientAMMONIA

Label structure12 sections

Dosage and administration

Inhale a slight whiff to treat a "fainting spell"

Contacts and useful links#

PhoneLabel contact1-800-662-3435

Label contents#

Full prescribing information#

WARNINGS AND PRECAUTIONS SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ammonia 2 %

Purpose

OTC - PURPOSE SECTION

Respiratory Stimulant

Use

INDICATIONS & USAGE SECTION

Respiratory stimulant used as a smelling salts to treat or prevent fainting.

Warnings

WARNINGS SECTION

For external use only. Avoid eye contact with liquid vapors. Avoid inhaling more than a slight whiff. May cause irritation if excess is inhaled.

If pregnant or nursing a baby

OTC - ASK DOCTOR SECTION

seek the advice of a doctor before using this product.

Keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Inhale a slight whiff to treat a "fainting spell"

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ammonium Carbonate, Sodium Carbonate

Other Information

OTHER SAFETY INFORMATION

Flammable: Keep away from spark, heat or flame. Keep tightly closed at room temperature not to exceed 30C (86F).

Questions or Comments?

OTC - QUESTIONS SECTION

1-800-662-3435

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label RAW

31 ml NDC 73395-197

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1437494	Ammonia (Nasal)	ammonia 20 MG/ML Nasal Inhalant	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1437494	ammonia 2 % Nasal Inhalant	PSN	1
1437494	ammonia 20 MG/ML Nasal Inhalant	SCD	1
1437494	ammonia 2 % Nasal Inhalant	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73395-197-01	2022-01-28	C162847	48780-1	d6a99b39-4772-a426-e053-dadaa90af4c2	Ammonia Sport RAW

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73395-197-01	AmmoniaSport RAW	31 mL in 1 BOTTLE, PLASTIC	LIQUID	31		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73395-197	AMMONIASPORT RAW (AMMONIA 2%) LIQUID [AMMONIASPORT LLC]	1	Legacy NDC, 1 package rows	20200919_af90c65b-cdfc-24c0-e053-2a95a90a7249.zip

Products#

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

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

AmmoniaSport RAW
Ammonia 2%
AMMONIUM CARBONATE
AMMONIA
SODIUM CARBONATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73395-197	73395-197-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
AMMONIUM CARBONATE	NJ5VT0FKLJ	IACT
AMMONIA	5138Q19F1X	ACTIB
SODIUM CARBONATE	45P3261C7T	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
af90c6c2-39a0-333b-e053-2995a90ac542			af90c65b-cdfc-24c0-e053-2a95a90a7249	2020-09-18	Warnings	Exact identifier spl id: af90c6c2-39a0-333b-e053-2995a90ac542 spl set id: af90c65b-cdfc-24c0-e053-2a95a90a7249

Reported adverse events (FAERS/openFDA)#

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

AmmoniaSport RAW