Ammonia
- Manufacturer
- McKesson
- Effective date
- 2021-09-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 23:42:16
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients (each inhalant)
Ammonia (15%)
OTC - PURPOSE SECTION
Purpose
Inhalant
INDICATIONS & USAGE SECTION
Uses To prevent or treat fainting.
WARNINGS SECTION
Warnings
For external use only.
Do not use if you have breathing problems such as asthma or emphysema.
OTC - STOP USE SECTION
Stop use and ask a doctor if condition persists.
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 right away.
DOSAGE & ADMINISTRATION SECTION
Directions Hold inhalant away from face and crush between thumb and forefinger. Carefully
approach crushed inhalant to nostrils of affected person.
OTHER SAFETY INFORMATION
Other Information Store at room temperature away from light.
INACTIVE INGREDIENT SECTION
Inactive Ingredients Alcohol USP, FD&C Red Dye # 40, Lavender Oil FCC, Lemon Oil FCC,
Nutmeg Oil FCC, Purified Water USP.
OTC - QUESTIONS SECTION
Questions? Call 1-800-777-4908
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC 68599-7100-1
McKesson
Ammonia Inhalants
15% - 35% Strength
Prevent or Treat Fainting
Net Contents
0.01 fl oz
(0.3 mL)
MFR# 10104
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68599-7100-1 | Ammonia | 0.15 g in 1 BOX | AEROSOL | 0.15 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68599-7100 | AMMONIA (INHALANT) AEROSOL [MCKESSON] | 3 | Legacy NDC, 1 package rows | 20210904_9c4865b7-6d76-7605-e053-2a95a90a1b3f.zip |
Products#
Every source-derived product name is available through these pages.
- Ammonia
- Inhalant
- ALCOHOL
- FD&C RED NO. 40
- LAVENDER OIL
- NUTMEG OIL
- WATER
- LEMON OIL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 68599-7100 | 68599-7100-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | IACT |
| FD&C RED NO. 40 | WZB9127XOA | IACT |
| LAVENDER OIL | ZBP1YXW0H8 | IACT |
| NUTMEG OIL | Z1CLM48948 | IACT |
| WATER | 059QF0KO0R | IACT |
| LEMON OIL | I9GRO824LL | IACT |
| AMMONIA | 5138Q19F1X | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| cb090ad6-5323-3f20-e053-2995a90aa2a2 | 9c4865b7-6d76-7605-e053-2a95a90a1b3f | 2021-09-02 | Warnings | cb090ad6-5323-3f20-e053-2995a90aa2a2 9c4865b7-6d76-7605-e053-2a95a90a1b3f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.


