| Product NDC: | 61252-3005 | 
| Proprietary Name: | Nicotine UN1654 | 
| Non Proprietary Name: | Nicotine UN1654 | 
| Active Ingredient(s): | 1 L/L & nbsp; Nicotine UN1654 | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 61252-3005 | 
| Labeler Name: | Nicobrand LTD | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER | 
| Start Marketing Date: | 19970711 | 
| Package NDC: | 61252-3005-1 | 
| Package Description: | 1 L in 1 DRUM (61252-3005-1) | 
| NDC Code | 61252-3005-1 | 
| Proprietary Name | Nicotine UN1654 | 
| Package Description | 1 L in 1 DRUM (61252-3005-1) | 
| Product NDC | 61252-3005 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Nicotine UN1654 | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 19970711 | 
| Marketing Category Name | UNAPPROVED DRUG OTHER | 
| Labeler Name | Nicobrand LTD | 
| Substance Name | NICOTINE | 
| Strength Number | 1 | 
| Strength Unit | L/L | 
| Pharmaceutical Classes | Cholinergic Nicotinic Agonist [EPC],Nicotine [Chemical/Ingredient] |