Ammonia Inhalant

Manufacturer
Moore Medical LLC | James Alexander Corp.
Effective date
2021-09-20
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 22:35:18

Label at a glance#

ProductAmmonia Inhalant
Active ingredientAMMONIA
Label structure12 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: (Each Inhalant)
Ammonia 15%

OTC - PURPOSE SECTION

Purpose
Inhalant

INDICATIONS & USAGE SECTION

Uses: To treat or to prevent 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 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 800-234-1464 Monday – Friday, 8:00am – 8:00pm [ET].

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Reorder No. 10104
Moore Medical
Supporting Health & Care
UPN# 0-0607415-10104-1
Moore Brand Ammonia Inhalants
100 Inhalants 0.01 fl. Oz. (0.3mL) each
Use to prevent fainting
For inhalation only
Individually wrapped

10104 Box10104 Box

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55670-710-012020-03-28C16284748780-19d75b9d0-c3f7-f424-e053-dadaa90a57ceMoore Ammonia Inhalants
55670-710-012020-01-31C16284748780-19d75b9d0-c3f7-f424-e053-dadaa90a57ceMoore Ammonia Inhalants

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55670-71055670-710-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
cc6eb737-6715-7cd2-e053-2995a90af54c5f261011-eec3-59fd-e053-2a91aa0a8e542021-09-20WarningsExact identifier
spl id: cc6eb737-6715-7cd2-e053-2995a90af54c
spl set id: 5f261011-eec3-59fd-e053-2a91aa0a8e54

Reported adverse events (FAERS/openFDA)#

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