LRNASH SMELLING SALTS

Manufacturer: Shenzhen Tie Gou Li Trading Co., Ltd.
Effective date: 2025-05-29
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 01:01:55

Label at a glance#

ProductLRNASH SMELLING SALTS

Active ingredientAMMONIUM CARBONATE

Label structure11 sections

Contacts and useful links#

PhonePoison Help1-800-222-1222

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ammonium Carbonate 15%

OTC - PURPOSE SECTION

Reflex stlmulant

INDICATIONS & USAGE SECTION

Uses To prevent or treat fainting,enhancealertness

WARNINGS SECTION

Keep away from the Eyes.
For external use only.
Stop use and ask a doctor if condition persists.

OTC - DO NOT USE SECTION

lf face is flush
in or near the eyes
lf you have breathing problems such as asthma or emphysema.

OTC - WHEN USING SECTION

Keep away from the Eyes,
For external use only.

OTC - STOP USE SECTION

Patient is non-responsive
condition lasts

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.1-800-222-1222

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older.
Hold the bottle 6 inches away from yournose,take a quick gentle sniff.
Close the cap tightly after each use.

INACTIVE INGREDIENT SECTION

Silica Silylate
Sea Salt
Ammonium Hydroxide
Carbonic Acid
Ammonium Fluorosilicate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
85405-001-01	LRNASH SMELLING SALTS	1 in 1 BOX	GRANULE	1		2
85405-001-01	LRNASH SMELLING SALTS	50 g in 1 BOTTLE	GRANULE	50		2

Products#

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

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

LRNASH SMELLING SALTS
Ammonium Carbonate
AMMONIUM HEXAFLUOROSILICATE
SEA SALT
AMMONIUM CATION
AMMONIA
CARBON DIOXIDE
SILANAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85405-001	85405-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
AMMONIUM HEXAFLUOROSILICATE	1X545W620G	IACT
SEA SALT	87GE52P74G	IACT
AMMONIUM CARBONATE	NJ5VT0FKLJ	ACTIB
AMMONIA	5138Q19F1X	IACT
CARBON DIOXIDE	142M471B3J	IACT
SILANAMINE	DO19I45F4L	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
36533b98-c699-e637-e063-6294a90a34d7			310df856-d50f-716e-e063-6394a90a7c03	2025-05-29	Warnings	Exact identifier spl id: 36533b98-c699-e637-e063-6294a90a34d7 spl set id: 310df856-d50f-716e-e063-6394a90a7c03

Reported adverse events (FAERS/openFDA)#

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