| Product NDC: | 50499-300 |
| Proprietary Name: | Dr MINERAL Anti-Itch |
| Non Proprietary Name: | SODIUM CHLORIDE |
| Active Ingredient(s): | .05; .7 mL/100mL; mL/100mL & nbsp; SODIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50499-300 |
| Labeler Name: | MineralBio |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100220 |
| Package NDC: | 50499-300-10 |
| Package Description: | 100 mL in 1 BOTTLE, SPRAY (50499-300-10) |
| NDC Code | 50499-300-10 |
| Proprietary Name | Dr MINERAL Anti-Itch |
| Package Description | 100 mL in 1 BOTTLE, SPRAY (50499-300-10) |
| Product NDC | 50499-300 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM CHLORIDE |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20100220 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | MineralBio |
| Substance Name | MENTHOL; SODIUM CHLORIDE |
| Strength Number | .05; .7 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |