Smelling Salt

Manufacturer
Shenzhen Chihai Trading Co., Ltd.
Effective date
2025-05-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:38:56

Label at a glance#

ProductSmelling Salt
Active ingredientAMMONIA
Label structure12 sections

Dosage and administration

1.Hold bottle 10-15 cm from nostrils and inhale slowly 1-2 times. 2. Seal tightly after each use to prevent prolonged exposure.

Storage and handling

Store at 15-25°C in a dark, dry place.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ammonia (15%)

Purpose

OTC - PURPOSE SECTION

Inhalant

Use

INDICATIONS & USAGE SECTION

To prevent or treat fainting.

Warnings

WARNINGS SECTION

Avoid contact with skin or eyes. Rinse immediately with water for
15 minutes if exposed.
Flammable. Keep away from heat, flames, or sparks.
For emergency use only. Not a substitute for professional medical

Do not use

OTC - DO NOT USE SECTION

1.Individuals with asthma or chronic respiratory conditions.
2.Children under 2 years of age.

OTC - WHEN USING SECTION

Avoid repeated inhalation. Do not use more than 2 times per
application.

OTC - STOP USE SECTION

Stop use and ask a doctor if allergic reaction (Rash, Swelling) or
persistent irritation occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Store in a cool, dry place inaccessible to children. Swallowing may cause poisoning.

Directions

DOSAGE & ADMINISTRATION SECTION

1.Hold bottle 10-15 cm from nostrils and inhale slowly 1-2 times.
2. Seal tightly after each use to prevent prolonged exposure.

Other information

STORAGE AND HANDLING SECTION

Store at 15-25°C in a dark, dry place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cotton and Peppermint Flavou

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85670-001SMELLING SALT POWDER [SHENZHEN CHIHAI TRADING CO., LTD.]2Unmatched20250521_3496bc37-d486-82f5-e063-6394a90a4809.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85670-00185670-001-01

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
NameUNIIKind
COTTON70LDW53ROOIACT
MENTHA ARVENSIS LEAF OIL1AEY1M553NIACT
AMMONIA5138Q19F1XACTIB

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
48ca3a19-d81b-5ece-e063-6294a90a13cf3496bc37-d486-82f5-e063-6394a90a48092026-01-19WarningsExact identifier
spl set id: 3496bc37-d486-82f5-e063-6394a90a4809

Reported adverse events (FAERS/openFDA)#

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