FDA.reportPublic FDA data

Shock-X Ammonia Inhalant

Manufacturer
Platinum Trident Enterprise
Effective date
2025-06-08
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:02:34

Label at a glance#

ProductShock-X Ammonia Inhalant
Active ingredientAMMONIA
Label structure9 sections

Indications and uses

To prevent or treat fainting.

Dosage and administration

Hold inhalant away from face and slowly approach inhalant to nostrils and inhale. Avoid contact with eyes and skin.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ammonia (15%)

Purpose

OTC - PURPOSE SECTION

Inhalant

Uses

INDICATIONS & USAGE SECTION

To prevent or treat fainting.

Warnings

WARNINGS SECTION

For external use only.

OTC - ASK DOCTOR SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

OTHER SAFETY INFORMATION

If swallowed, seek medical help or contact a Poison Control Center right away.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or nursing, seek the advice of a doctor before using this product.

Directions

DOSAGE & ADMINISTRATION SECTION

Hold inhalant away from face and slowly approach inhalant to nostrils and inhale. Avoid contact with eyes and skin.

Other Information

OTHER SAFETY INFORMATION

Store at room temperature away from light.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Alcohol, Cotton, Peppermint Oil, Water.

Questions

OTC - QUESTIONS SECTION

Contact us at support@shock-x.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85570-111185570-1111-1, 85570-1111-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
SEA SALT87GE52P74GIACT
PEPPERMINT OILAV092KU4JHIACT
AMMONIA5138Q19F1XACTIB
AMMONIUM CARBONATENJ5VT0FKLJIACT

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
421b75a4-8f8f-f304-e063-6294a90a42903365af8c-78cb-4978-e063-6394a90a2e872025-10-26WarningsExact identifier
spl set id: 3365af8c-78cb-4978-e063-6394a90a2e87

Reported adverse events (FAERS/openFDA)#

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