87957-005

Manufacturer
Hubei Minxin Pharmaceutical Co., Ltd.
Effective date
2026-08-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-01 13:02:04

Label at a glance#

ProductNrmrqz SMELLING SALTS
Active ingredientMENTHOL
Label structure13 sections

Dosage and administration

Hold bottle 10-15 cm (4-6 inches) from nostrils. Inhale gently. Do not place directly inside the nostrils. Do not inhale for more than 2 seconds per use. Do not use more than once every 60 minutes. Do not use more than 10 times per day. Use only as needed. If symptoms persist, consult a healthcare professional.

Storage and handling

Store in a cool, dry place at 15-25°C (59-77°F). Avoid freezing, excessive heat above 40°C (104°F), and direct sunlight. Do not use if safety seal under cap is broken .

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 15%

Purpose

OTC - PURPOSE SECTION

For the temporary stimulation of the senses to restore alertness.

Use

INDICATIONS & USAGE SECTION

For the temporary stimulation of the senses to restore alertness.

Warnings

WARNINGS SECTION

For inhalation use only.
Do not ingest or apply to skin.
Avoid direct contact with eyes.
If contact occurs, rinse thoroughly with water for 15 minutes.
Use only as directed. Misuse may be harmful.
Use in a well-ventilated area.
Do not use in enclosed spaces.
Prolonged exposure may cause irritation.
Discontinue use if discomfort occurs.
Possible side effects include nasal irritation, coughing, or shortness of breath.
If symptoms persist, discontinue use and consult a doctor.

Do not use

OTC - DO NOT USE SECTION

If you have respiratory conditions such as asthma or emphysema.
If you have heart disease or high blood pressure.
If you are allergic to ammonia or strong odors.

When Using

OTC - WHEN USING SECTION

Avoid contact with eyes, ears, and mouth.
If product gets into eyes, rinse thoroughly with water for 15 minutes.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Ask Doctor

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately at 1-800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

Hold bottle 10-15 cm (4-6 inches) from nostrils.
Inhale gently. Do not place directly inside the nostrils.
Do not inhale for more than 2 seconds per use.
Do not use more than once every 60 minutes.
Do not use more than 10 times per day.
Use only as needed. If symptoms persist, consult a healthcare professional.

Other information

STORAGE AND HANDLING SECTION

Store in a cool, dry place at 15-25°C (59-77°F).
Avoid freezing, excessive heat above 40°C (104°F), and direct sunlight.
Do not use if safety seal under cap is broken .

Inactive ingredients

INACTIVE INGREDIENT SECTION

Eucalyptus Oil, Sea Salt, Alcohol, Ammonium Carbonate, Peppermint Oil

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1515

Products#

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87957-00587957-005-01

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Nrmrqz SMELLING SALTSMENTHOL 15% SMELLING SALTSHubei Minxin Pharmaceutical Co., Ltd.5a27f471-e54e-cbbf-e063-6394a90aa8042026-08-28WarningsExact identifier
ndc (package): 87957-005-01
ndc (product): 87957-005
ndc11 (package): 87957000501
spl id: 5a27f471-e54f-cbbf-e063-6394a90aa804
spl set id: 5a27f471-e54e-cbbf-e063-6394a90aa804

Reported adverse events (FAERS/openFDA)#

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