Product NDC: | 52124-3201 |
Proprietary Name: | Ammonia Pad |
Non Proprietary Name: | AMMONIA |
Active Ingredient(s): | 10 mL/100mL & nbsp; AMMONIA |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | INHALANT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52124-3201 |
Labeler Name: | Genuine First Aid, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110404 |
Package NDC: | 52124-3201-1 |
Package Description: | .5 mL in 1 PACKET (52124-3201-1) |
NDC Code | 52124-3201-1 |
Proprietary Name | Ammonia Pad |
Package Description | .5 mL in 1 PACKET (52124-3201-1) |
Product NDC | 52124-3201 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AMMONIA |
Dosage Form Name | INHALANT |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 20110404 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Genuine First Aid, LLC |
Substance Name | AMMONIA |
Strength Number | 10 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |