| Product NDC: | 61787-482 |
| Proprietary Name: | Nasal Ease Allergy Reliever |
| Non Proprietary Name: | Potassium Dichromate |
| Active Ingredient(s): | 200 [AU]/5.1g & nbsp; Potassium Dichromate |
| Administration Route(s): | NASAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 61787-482 |
| Labeler Name: | Health Care Products |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20090803 |
| Package NDC: | 61787-482-50 |
| Package Description: | 1 BOTTLE in 1 BOX (61787-482-50) > 5.1 g in 1 BOTTLE |
| NDC Code | 61787-482-50 |
| Proprietary Name | Nasal Ease Allergy Reliever |
| Package Description | 1 BOTTLE in 1 BOX (61787-482-50) > 5.1 g in 1 BOTTLE |
| Product NDC | 61787-482 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Potassium Dichromate |
| Dosage Form Name | POWDER |
| Route Name | NASAL |
| Start Marketing Date | 20090803 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Health Care Products |
| Substance Name | POTASSIUM DICHROMATE |
| Strength Number | 200 |
| Strength Unit | [AU]/5.1g |
| Pharmaceutical Classes |