Indications and uses
• For temporary relief of lightheadedness or faintness • As a respiratory stimulant following fainting
• For temporary relief of lightheadedness or faintness • As a respiratory stimulant following fainting
Directions • Hold container away from nose • Briefly waft vapors toward the nose • Use as needed • Do not exceed 2 inhalations per use
Active Ingredient: Ammonia 15%
Purpose: Inhalant
• For temporary relief of lightheadedness or faintness
• As a respiratory stimulant following fainting
For external use only.
Do not use
• If you have respiratory conditions such as asthma or emphysema unless directed by a doctor
When using this product
• Avoid prolonged or repeated inhalation
• Do not apply directly to the nostrils
• Avoid contact with eyes and skin
Stop use and ask a doctor if
• Symptoms persist or worsen
• Irritation or discomfort occurs
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Directions
• Hold container away from nose
• Briefly waft vapors toward the nose
• Use as needed
• Do not exceed 2 inhalations per use
Alcohol, Cotton
• Store at room temperature (15–25°C / 59–77°F)
• Keep container tightly closed
• Protect from light
• Expiration date: see batch number on bottle base
For the temporary relief of lightheadedness or fainting.
Keep out of reach of children.
Front, side, and back panels of the Palinoia Ammonia Inhalant retail carton are shown above.
The labeling includes the product name, NDC number, net weight, Drug Facts panel with active ingredient (ammonia solution 15%), purpose, uses, warnings, directions, inactive ingredients, storage instructions, expiration information, and distributor details.
PALINOIA AMMONIA INHALANT
Net Weight: 40 g
NDC: 87176-001-02
Drug Facts
Active ingredient
Ammonia solution (15%) — Inhalant
Purpose
Inhalant
Uses
• For temporary relief of lightheadedness or faintness
• As a respiratory stimulant following fainting
Warnings
For external use only.
Do not use if you have respiratory conditions such as asthma or emphysema unless directed by a doctor.
When using this product
• Avoid prolonged or repeated inhalation
• Do not apply directly to the nostrils
• Avoid contact with eyes and skin
Stop use and ask a doctor if
• Symptoms persist or worsen
• Irritation or discomfort occurs
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Directions
• Hold container away from nose
• Briefly waft vapors toward the nose
• Use as needed
• Do not exceed 2 inhalations per use
Other information
• Store at room temperature
• Keep container tightly closed
• Expiration date: see batch number on bottle base
Inactive ingredients
Alcohol, cotton
Questions or comments?
info@palinoiadiagnostics.com
Distributed by:
CenterOblivion LLC
Sheridan, WY 82801 USA
Made in China
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0198715391244 | GTIN-13: 0198715391244 EAN-13: 0198715391244 GTIN-12: 198715391244 UPC-A: 198715391244 GTIN storage (14 digits): 00198715391244 | AMMONIA INHALANT_Box.jpg |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 87176-002-01 | Palinoia Ammonia Inhalant | 40 g in 1 BOTTLE | INHALANT | 40 | 3 | |
| 87176-002-02 | Palinoia Ammonia Inhalant | 1 in 1 BOX | INHALANT | 1 | 3 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 87176-002 | 87176-002-01, 87176-002-02 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| COTTON | 70LDW53ROO | IACT |
| AMMONIA | 5138Q19F1X | ACTIB |
| ALCOHOL | 3K9958V90M | IACT |
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 2 | 2025-10-30 | monthly-update | 2026-06-03 18:00:40 |
| 1 | 2025-10-30 | monthly-update | 2026-06-03 17:51:52 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 5856c130-4114-6037-e063-6294a90ab284 | 42699816-1ae2-cfea-e063-6394a90aec1f | 2026-08-05 | Warnings | 42699816-1ae2-cfea-e063-6394a90aec1f |
Adverse event summaries are temporarily unavailable. Other product information remains available.