Aromatic Ammonia Spirit

Manufacturer
Humco Holding Group, inc | Humco Holding Group, Inc.
Effective date
2022-03-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:05:49

Label at a glance#

ProductAromatic Ammonia Spirit
Active ingredientAMMONIA
Label structure11 sections

Dosage and administration

 Inhale a slight whiff to treat a "faining spell"

Label contents#

Full prescribing information#

WARNINGS AND PRECAUTIONS SECTION

 Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

 Ammonia 2 %

Purpose

OTC - PURPOSE SECTION

 Respiratory Stimulant

Indication

INDICATIONS & USAGE SECTION

Respiratory stimulant used as a smelling salts to treat or prevent fainting.

Warnings

WARNINGS SECTION

 For external use only. Avoid eye contact with liquid vapors. Avoid inhaling more than a slight whiff. May cause irritation if excess is inhaled.

If pregnant or nursing a baby

OTC - ASK DOCTOR SECTION

 seek the advice of a doctor before using this product.

Keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

 In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

 Inhale a slight whiff to treat a "faining spell"

Inactive Ingredients

INACTIVE INGREDIENT SECTION

 Ammonium Carbonate, Ethyl Alcohol 656%, Lavender Oil, Lemon Oil Terpenless, Myristica Oil and Purified Water.

Other Information

OTHER SAFETY INFORMATION

 Flammable: Keep away from spark, heat or flame. Keep tightly closed at room temperature not toexceed 30C (86F).

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0395-91010395-9101-92

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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
da6eac43-f418-8f1e-e053-2a95a90af4af60402908-5519-5970-e053-2a91aa0ab3612022-03-17WarningsExact identifier
spl id: da6eac43-f418-8f1e-e053-2a95a90af4af
spl set id: 60402908-5519-5970-e053-2a91aa0ab361

Reported adverse events (FAERS/openFDA)#

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