Product NDC: | 50499-200 |
Proprietary Name: | Dr MINERAL Anti-Itch Spray |
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: | 50499-200 |
Labeler Name: | MineralBio |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100220 |
Package NDC: | 50499-200-10 |
Package Description: | 100 mL in 1 BOTTLE, SPRAY (50499-200-10) |
NDC Code | 50499-200-10 |
Proprietary Name | Dr MINERAL Anti-Itch Spray |
Package Description | 100 mL in 1 BOTTLE, SPRAY (50499-200-10) |
Product NDC | 50499-200 |
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 |