Label at a glance#

ProductSummit Smelling Salts

Active ingredientAMMONIA

Label structure12 sections

Storage and handling

OTHER INFORMATION: Store at room temperature away from light and moisture.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ammonia (15%)

OTC - PURPOSE SECTION

Inhalant

INDICATIONS & USAGE SECTION

To prevent or treat fainting.

WARNINGS SECTION

WARNINGS: For external use only. Avoid contact with skin, eyes, and mouth.

OTC - DO NOT USE SECTION

if allergic, pregnant or have respiratory conditions.

OTC - WHEN USING SECTION

INSTRUCTIONS:

1.Shake well before use.

2.Unscrew cap and hold at least 6 inches from nose.

3. Inhale slowly no more than 1-2 times per use.

4.Seal tightly and store in a dark, dry place at room temperature.

BEFORE USE:

Remove plastic seal, unscrew cap, and remove foil from mouth of bottle. Reseal lid after each use.

POTENCY PRESERVATION :

To maintain potency over time, always seal the lid tightly immediately after each use. Before each session, shake the bottle thoroughly to ensure optimal ammonia activation. For best experience, store the bottle in a dark, dry place at room temperature.

OTC - STOP USE SECTION

STOP USE AND ASK A DOCTOR if symptoms occur.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. If ingested, seek medical attention or contact Poison Control immediately.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Hold bottle at least 6 inches from nose and inhale slowly no more than 1-2 times per use. Avoid repeated inhalationy

STORAGE AND HANDLING SECTION

OTHER INFORMATION: Store at room temperature away from light and moisture.

INACTIVE INGREDIENT SECTION

Alcohol, Mint Flavor.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

85764-001-01

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	3
1299889	ammonia 150 MG/ML Nasal Inhalant	SCD	3
1299889	ammonia 0.045 GM per 0.3 ML Nasal Inhalant	SY	3
1299889	ammonia 0.3 ML Nasal Inhalant	SY	3
1299889	ammonia 15 % Nasal Inhalant	SY	3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
85764-001-01	Summit Smelling Salts	40 g in 1 BOX	INHALANT	40		3

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Summit Smelling Salts
AMMONIA
ALCOHOL
MINT

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85764-001	85764-001-01

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
AMMONIA	5138Q19F1X	ACTIB
ALCOHOL	3K9958V90M	IACT
MINT	FV98Z8GITP	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
Summit Smelling Salts	SUMMIT SMELLING SALTS	Washburn Ventures LLC	36b6ed08-4a98-6b31-e063-6394a90a6fb7	2025-06-16	Warnings	Exact identifier ndc (package): 85764-001-01 ndc (product): 85764-001 ndc11 (package): 85764000101 spl id: 37ae4331-f69c-aad0-e063-6394a90ab58d spl set id: 36b6ed08-4a98-6b31-e063-6394a90a6fb7

Reported adverse events (FAERS/openFDA)#

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

Summit Smelling Salts