Ammonia Inhalants

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Ammonia Inhalants
Generic name
AMMONIA INHALANTS
Manufacturer
James Alexander Corporation
Product type
HUMAN OTC DRUG
SPL set ID
b741afa6-e56c-4fbb-ada0-80b80aef72a7
SPL ID
a4d241dd-e857-4978-9112-0463a1fcf7d2
Version
4
Effective date
2019-01-31
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:14:00
Harmonized routes table
Harmonized routes
RESPIRATORY (INHALATION)

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Do not use if you have breathing problems such as asthma or emphysema. Stop use and ask a doctor if condition persists.

Reported adverse events (FAERS/openFDA)#

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