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OTC products · Product label record

Smelling Salts drug information

AMMONIA
Shenzhen Finona Information Technology Co., Ltd · RESPIRATORY (INHALATION)

Product NDC: 85839-005

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameAMMONIA
Labeler / manufacturerShenzhen Finona Information Technology Co., Ltd
RouteRESPIRATORY (INHALATION)
Drug classDrug class not supplied in source label
Product NDC85839-005
Label effective date2026-08-24

Official product label reference

Smelling Salts — Shenzhen Finona Information Technology Co., Ltd

This page contains 9 source sections for AMMONIA, respiratory (inhalation) route. Label set 3874ec89-0f1d-87b9-e063-6394a90a300a, version 5.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

For the temporary stimulation of the senses to restore alertness.

Purpose

Inhalant
Dosage and administration — label text
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. lfsymptoms persist, consult ahealthcare professional
Warnings
For inhalation use only. Do not ingest or apply to skin. Avoid direct contact with eyes. lf contact occurs, rinsethoroughly 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. lf symptoms persist, discontinue use and consult a doctor.
Active ingredient
Ammonia 15%
Do not use
It you have respiratory conditions such as asthma oremphysema. If you have heart disease or high blood pressure. If you are allergic to ammonia or strong odors.
While using this medicine
Avoid contact with eyes, ears, and mouth. lf product gets into eyes, rinse thoroughly with water for 15 minutes. Stop use and ask a doctor ifirritation or rash occurs. These may be signs of a serious condition.
Child safety
Keep out of reach of children. lfswallowed, get medical help or contact a Poison Control centerimmediately at 1-800-222-1222
Inactive ingredient
Alcohol Cotton Peppermint Oil

Official sources and product identifiers

Substances listed: AMMONIA

RxNorm identifiers: 1299889

Package NDC codes

85839-005-01

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.