Snap Labs 20-Count Ammonia Inhalants

Manufacturer: Brined LLC d/b/a Snap Labs
Effective date: 2025-12-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:21:15

Label at a glance#

ProductSnap Labs 20-Count Ammonia Inhalants

Active ingredientAMMONIA

Label structure9 sections

Indications and uses

Helps prevent or treat fainting.

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ammonia (15%)...Inhalant

Purpose

OTC - PURPOSE SECTION

Inhalant

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

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Do not use

OTC - DO NOT USE SECTION

Do not use if you have breathing problems such as asthma or emphysema.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients Alcohol USP, FD&C Red Dye # 40, Lavender Oil FCC, Lemon Oil FCC, Nutmeg Oil FCC, Purified Water USP.

Uses

INDICATIONS & USAGE SECTION

Helps prevent or treat fainting.

Drug Facts Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DRUG FACTS LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1299889	ammonia 15 % Nasal Inhalant	PSN	1
2728560	Snap Labs 150 MG/ML Nasal Inhalant	PSN	1
2728560	ammonia 150 MG/ML Nasal Inhalant [Snap Labs]	SBD	1
1299889	ammonia 150 MG/ML Nasal Inhalant	SCD	1
1299889	ammonia 0.045 GM per 0.3 ML Nasal Inhalant	SY	1
1299889	ammonia 0.3 ML Nasal Inhalant	SY	1
1299889	ammonia 15 % Nasal Inhalant	SY	1
2728560	Snap Labs 150 MG/ML Nasal Inhalant	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
87270-002-01	Snap Labs 20-Count Ammonia Inhalants	1 in 1 BAG	INHALANT	1		1
87270-002-01	Snap Labs 20-Count Ammonia Inhalants	20 in 1 JAR	INHALANT	20		1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Snap Labs 20-Count Ammonia Inhalants
Ammonia Inhalants
LAVENDER OIL
LEMON OIL
NUTMEG OIL
FD&C RED NO. 40
AMMONIA
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
87270-002	87270-002-01
46414-3333

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
LAVENDER OIL	ZBP1YXW0H8	IACT
LEMON OIL	I9GRO824LL	IACT
NUTMEG OIL	Z1CLM48948	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
AMMONIA	5138Q19F1X	ACTIB
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Snap Labs 20-Count Ammonia Inhalants	AMMONIA INHALANTS	Brined LLC d/b/a Snap Labs	4575d816-b08f-13fb-e063-6294a90af3ba	2025-12-08	Warnings	Exact identifier ndc (package): 87270-002-01 ndc (product): 87270-002 ndc11 (package): 87270000201 spl id: 4575d816-b090-13fb-e063-6294a90af3ba spl set id: 4575d816-b08f-13fb-e063-6294a90af3ba
Ammonia Inhalants	AMMONIA INHALANTS	James Alexander Corporation	b741afa6-e56c-4fbb-ada0-80b80aef72a7	2019-01-31	Warnings	Exact identifier ndc (product): 46414-3333

Reported adverse events (FAERS/openFDA)#

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