| Product NDC: | 47219-311 |
| Proprietary Name: | Nyloxin |
| Non Proprietary Name: | NAJA NAJA VENOM |
| Active Ingredient(s): | 4 [hp_X]/mL & nbsp; NAJA NAJA VENOM |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 47219-311 |
| Labeler Name: | Receptopharm Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20100823 |
| Package NDC: | 47219-311-02 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 BOX (47219-311-02) > 60 mL in 1 BOTTLE, WITH APPLICATOR |
| NDC Code | 47219-311-02 |
| Proprietary Name | Nyloxin |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 BOX (47219-311-02) > 60 mL in 1 BOTTLE, WITH APPLICATOR |
| Product NDC | 47219-311 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | NAJA NAJA VENOM |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100823 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Receptopharm Inc. |
| Substance Name | NAJA NAJA VENOM |
| Strength Number | 4 |
| Strength Unit | [hp_X]/mL |
| Pharmaceutical Classes |