| 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 |