87957-015

Manufacturer
Hubei Minxin Pharmaceutical Co., Ltd.
Effective date
2026-09-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-15 03:01:47

Label at a glance#

ProductWXMX 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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136980507550038GTIN-13: 6980507550038
EAN-13: 6980507550038
GTIN storage (14 digits): 06980507550038
51b0675f2232cebaa6496f0b543b4d1c.jpg

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87957-01587957-015-01

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 4 of 44 · 878 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Biofreeze Roll-On and Overnight Roll-OnMENTHOLReckitt Benckiser LLC4d3dcb8f-2075-6bbc-e063-6394a90a49922026-05-15WarningsName fallback
generic name: MENTHOL
Biofreeze Roll-OnMENTHOLReckitt Benckiser LLCebbbe9cb-b1ce-4dac-9fca-f54a2470c4fb2026-05-15WarningsName fallback
generic name: MENTHOL
Biofreeze Precision Relief PenMENTHOLReckitt Benckiser LLCb4cc1db5-a33f-17bc-e053-2995a90ab7eb2026-05-15WarningsName fallback
generic name: MENTHOL
PERFORM COOL AND SOOTHING PAIN RELIEVING ROLL-ONMENTHOLReckitt Benckiser LLC8af185ad-719e-4684-89c0-9c17c12774992026-05-15WarningsName fallback
generic name: MENTHOL
PERFORM COOL and SOOTHING PAIN RELIEVINGMENTHOLReckitt Benckiser LLCef158f63-2d75-47a3-b94a-2d821d5118632026-05-15WarningsName fallback
generic name: MENTHOL
OVERNIGHT RELIEF Gel-PatchMENTHOLShanghai Chuangshi Medical Technology (Group) Co., Ltd.2c6c4737-dff3-6382-e063-6294a90a412c2026-05-14WarningsName fallback
generic name: MENTHOL
Pain ReliefMENTHOLShanghai Chuangshi Medical Technology (Group) Co., Ltd.3ed34e65-9d74-daff-e063-6394a90a94c72026-05-14WarningsName fallback
generic name: MENTHOL
MENTHOL PAIN RELIEF Gel-PatchMENTHOLShanghai Chuangshi Medical Technology (Group) Co., Ltd.0e6a09cc-7986-f851-e063-6294a90aff672026-05-14WarningsName fallback
generic name: MENTHOL
OVERNIGHT RELIEF Gel-PatchMENTHOLShanghai Chuangshi Medical Technology (Group) Co., Ltd.f1041b25-eb09-e43d-e053-2995a90a073a2026-05-14WarningsName fallback
generic name: MENTHOL
Elastic Relief StripMENTHOLShanghai Chuangshi Medical Technology (Group) Co., Ltd.f103cf8a-a285-28d1-e053-2995a90ae70e2026-05-14WarningsName fallback
generic name: MENTHOL
Halls Honey LemonMENTHOLMondelez Global LLCaec46410-ffb1-4db4-b232-82110c562f692026-05-13WarningsName fallback
generic name: MENTHOL
Pain Relief Gel-Roll OnMENTHOLTrifecta Pharmaceuticals USA51b403dc-fc9b-0cad-e063-6394a90af0812026-05-13WarningsName fallback
generic name: MENTHOL
BiofreezeMENTHOLReckitt Benckiser LLC5edddb99-6596-4a3b-b361-1cc04d032c312026-05-13WarningsName fallback
generic name: MENTHOL
BiofreezeMENTHOLReckitt Benckiser LLC684faf63-5e44-4471-8384-e8fa7c0d842a2026-05-13WarningsName fallback
generic name: MENTHOL
BiofreezeMENTHOLReckitt Benckiser LLC4c798b06-6ee5-41d1-8a14-f6889512ade32026-05-13WarningsName fallback
generic name: MENTHOL
BIOFREEZEMENTHOLReckitt Benckiser LLC83d5c2f2-2413-4d28-83b2-0808d0917b4d2026-05-13WarningsName fallback
generic name: MENTHOL
BiofreezeMENTHOLReckitt Benckiser LLC10a8face-47da-ebbe-e063-6294a90a42fe2026-05-13WarningsName fallback
generic name: MENTHOL
Biofreeze Foot CreamMENTHOLReckitt Benckiser LLC32450cbf-4ed4-402b-a30e-e08a17bba3fb2026-05-13WarningsName fallback
generic name: MENTHOL
BiofreezeMENTHOLReckitt Benckiser LLCa227213b-e89f-7144-e053-2a95a90a7e742026-05-13WarningsName fallback
generic name: MENTHOL
BiofreezeMENTHOLReckitt Benckiser LLC00bb462a-27d0-6f74-e063-6394a90a90ec2026-05-13WarningsName fallback
generic name: MENTHOL

Reported adverse events (FAERS/openFDA)#

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