Content
One prep pad saturated with 10% ammonia
Ammonia Pad
FDA Label NDC 52124-3201
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Genuine First Aid, Llc for the product Ammonia Pad (NDC 52124-3201). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding content, purpose, uses, caution, inactive ingredients, directions, otc - keep out of reach of children, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
prevent or treat fainting
Uses
Uses to arouse the consciousness of a fainted victim with the vigorous smell of the ammonia in the pad. For external use only.
Caution
Do not swallow. Keep away from eyes; wash with plenty of water if contacted.
Inactive Ingredients
Purified water.
Directions
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
Keep out of reach of children
Package Label.Principal Display Panel
Ammonia Inhalant Pad
GFA Production Xiamen Co., Ltd
www.gfaproduction.com
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
Ammonia Inhalant Pads (Ammonia)
Ammonia Inhalant Pads (Ammonia Box)
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