Ammonia Pad

Manufacturer: Genuine First Aid, LLC
Effective date: 2011-04-04
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:27:38

Label at a glance#

ProductAmmonia Pad

Active ingredientAMMONIA

Label structure10 sections

Indications and uses

Uses to arouse the consciousness of a fainted victim with the vigorous smell of the ammonia in the pad. For external use only.

Dosage and administration

Tear off a corner and wave it under the victim's nose that has fainted or is on the verge of unconsciousness.

Contacts and useful links#

Websitewww.gfaproduction.com

www.gfaproduction.com

Label contents#

Full prescribing information#

Content

OTC - ACTIVE INGREDIENT SECTION

One prep pad saturated with 10% ammonia

Purpose

OTC - PURPOSE SECTION

prevent or treat fainting

Uses

INDICATIONS & USAGE SECTION

Uses to arouse the consciousness of a fainted victim with the vigorous smell of the ammonia in the pad. For external use only.

Caution

WARNINGS SECTION

Do not swallow. Keep away from eyes; wash with plenty of water if contacted.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified water.

Directions

DOSAGE & ADMINISTRATION SECTION

Tear off a corner and wave it under the victim's nose that has fainted or is on the verge of unconsciousness.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ammonia Inhalant Pad

GFA Production Xiamen Co., Ltd
www.gfaproduction.com

GFA Production Xiamen Co., Ltd
No. 20 Huli Industrial Park, Meixi Road,
Tong'an, Xiamen, Fujian, China 361100

Wellkang Ltd t/a Wellkang Tech Consulting
Suite B, 29 Harley Street
LONDON W1G 9QR, England, United Kingdom

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ammonia Inhalant Pads

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ammonia Inhalant Pads

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52124-3201-1	2019-10-29	C162847	48780-1	960f7f55-c1e5-8e05-e053-dbdaa90a074a	Ammonia Inhalant Pad
52124-3201-2	2019-10-29	C162847	48780-1	960f7f55-c1e5-8e05-e053-dbdaa90a074a	Ammonia Inhalant Pad

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
52124-3201-1	Ammonia Pad	0.5 mL in 1 PACKET	INHALANT	0.5	1
52124-3201-2	Ammonia Pad	100 in 1 BOX	INHALANT	100	1
52124-3201-2	Ammonia Pad	0.5 mL in 1 PACKET	INHALANT	0.5	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52124-3201	AMMONIA PAD (AMMONIA) INHALANT [GENUINE FIRST AID, LLC]	1	Legacy NDC, 3 package rows	20110405_6a5a1fd9-3f97-4715-b462-c7a07aed8159.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
AMMONIA	ACTIVE INGREDIENT	5138Q19F1X	1
AMMONIA	ACTIVE MOIETY	5138Q19F1X	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Ammonia Pad
AMMONIA
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52124-3201	52124-3201-1, 52124-3201-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
AMMONIA	5138Q19F1X	ACTIB
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f155deda-b928-428a-b570-79d5d556b217			6a5a1fd9-3f97-4715-b462-c7a07aed8159	2011-04-04	Warnings	Exact identifier spl id: f155deda-b928-428a-b570-79d5d556b217 spl set id: 6a5a1fd9-3f97-4715-b462-c7a07aed8159

Reported adverse events (FAERS/openFDA)#

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