| Product NDC: | 52345-5001 |
| Proprietary Name: | NoSno |
| Non Proprietary Name: | XANTHAN GUM |
| Active Ingredient(s): | .05 mL/44mL & nbsp; XANTHAN GUM |
| Administration Route(s): | NASAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52345-5001 |
| Labeler Name: | K&J.C Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120303 |
| Package NDC: | 52345-5001-1 |
| Package Description: | 44 mL in 1 BOTTLE, WITH APPLICATOR (52345-5001-1) |
| NDC Code | 52345-5001-1 |
| Proprietary Name | NoSno |
| Package Description | 44 mL in 1 BOTTLE, WITH APPLICATOR (52345-5001-1) |
| Product NDC | 52345-5001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | XANTHAN GUM |
| Dosage Form Name | LIQUID |
| Route Name | NASAL |
| Start Marketing Date | 20120303 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | K&J.C Co., Ltd |
| Substance Name | XANTHAN GUM |
| Strength Number | .05 |
| Strength Unit | mL/44mL |
| Pharmaceutical Classes |